A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527191



Internal ID15107798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37206017..37212747hg38UCSC Ensembl
Innerchr6:37173793..37180523hg19UCSC Ensembl
Innerchr6:37281771..37288501hg18UCSC Ensembl
Innerchr6:37281771..37288501hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg386731
hg196731
hg186731
hg176731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703588
Samples
Known GenesTMEM217
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527191
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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