A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703858



Internal ID15440510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14064042..14088071hg38UCSC Ensembl
Innerchr6:14064273..14088302hg19UCSC Ensembl
Innerchr6:14172252..14196281hg18UCSC Ensembl
Innerchr6:14172252..14196281hg17UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3824030
hg1924030
hg1824030
hg1724030
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527420
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703858
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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