A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672006



Internal ID15408658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255491..4472353hg38UCSC Ensembl
Innerchr6:4255725..4472587hg19UCSC Ensembl
Innerchr6:4200724..4417586hg18UCSC Ensembl
Innerchr6:4200724..4417586hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38216863
hg19216863
hg18216863
hg17216863
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516402
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672006
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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