A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672193



Internal ID15062159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167269581..167357248hg38UCSC Ensembl
Innerchr6:167683069..167770736hg19UCSC Ensembl
Innerchr6:167603059..167690726hg18UCSC Ensembl
Innerchr6:167653480..167741147hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3887668
hg1987668
hg1887668
hg1787668
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517210
Supporting Variants
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672193
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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