A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700703



Internal ID15437355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81919019..81922532hg38UCSC Ensembl
Innerchr6:82628736..82632249hg19UCSC Ensembl
Innerchr6:82685455..82688968hg18UCSC Ensembl
Innerchr6:82685455..82688968hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383514
hg193514
hg183514
hg173514
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700703
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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