A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1630999



Internal ID15153386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29869415..29953350hg38UCSC Ensembl
Innerchr6:29837192..29921127hg19UCSC Ensembl
Innerchr6:29945171..30029106hg18UCSC Ensembl
Innerchr6:29945171..30029106hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3883936
hg1983936
hg1883936
hg1783936
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv442976
Supporting Variants
SamplesNA19239
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisWe used two computational approaches to identify CNVs: the hidden Markov model Birdseye, and an approach based on correlation between nearby probes across a population sample. To maximize the quality of reported findings, we ran duplicate experiments in independent labs, and report the CNVs that were observed in both experiments, in the same samples and at essentially identical genomic locations.
Platform[GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
Comments
ReferenceMcCarroll_et_al_2008
Pubmed ID18776908
Accession Number(s)nssv1630999
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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