A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674241



Internal ID15064207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31440051..31440136hg38UCSC Ensembl
Innerchr6:31407828..31407913hg19UCSC Ensembl
Innerchr6:31515807..31515892hg18UCSC Ensembl
Innerchr6:31515807..31515892hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3886
hg1986
hg1886
hg1786
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674241
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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