A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437633



Internal ID15382939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129004138..129004253hg38UCSC Ensembl
Outerchr8:129001954..129010011hg38UCSC Ensembl
Innerchr8:130016384..130016499hg19UCSC Ensembl
Outerchr8:130014200..130022257hg19UCSC Ensembl
Innerchr8:130085566..130085681hg18UCSC Ensembl
Outerchr8:130083382..130091439hg18UCSC Ensembl
Innerchr8:129972973..129973088hg16UCSC Ensembl
Outerchr8:129970789..129978846hg16UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg388058
hg198058
hg188058
hg168058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467514
SamplesNA18860
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)nsv437633
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