A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437679



Internal ID15382985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11912166..11914418hg38UCSC Ensembl
Outerchr3:11903805..11919376hg38UCSC Ensembl
Innerchr3:11953640..11955892hg19UCSC Ensembl
Outerchr3:11945279..11960850hg19UCSC Ensembl
Innerchr3:11928640..11930892hg18UCSC Ensembl
Outerchr3:11920279..11935850hg18UCSC Ensembl
Innerchr3:11928640..11930892hg16UCSC Ensembl
Outerchr3:11920279..11935850hg16UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3815572
hg1915572
hg1815572
hg1615572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467560
SamplesNA10838
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)nsv437679
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