A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv467580



Internal ID15381971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4700912..4707934hg38UCSC Ensembl
Outerchr11:4699974..4720724hg38UCSC Ensembl
Innerchr11:4722142..4729164hg19UCSC Ensembl
Outerchr11:4721204..4741954hg19UCSC Ensembl
Innerchr11:4678718..4685740hg18UCSC Ensembl
Outerchr11:4677780..4698530hg18UCSC Ensembl
Innerchr11:4686451..4693473hg16UCSC Ensembl
Outerchr11:4685513..4706263hg16UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3820751
hg1920751
hg1820751
hg1620751
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele OriginGermline
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437699
Supporting Variants
SamplesNA18914
Known Genes
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nssv467580
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer