A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698825



Internal ID15088791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52744866..52756806hg38UCSC Ensembl
Innerchr6:52609664..52621604hg19UCSC Ensembl
Innerchr6:52717623..52729563hg18UCSC Ensembl
Innerchr6:52717623..52729563hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3811941
hg1911941
hg1811941
hg1711941
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523124
Supporting Variants
Samples
Known GenesGSTA2, GSTA7P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698825
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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