A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706053



Internal ID15096019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36948130..36957998hg38UCSC Ensembl
Innerchr6:36915906..36925774hg19UCSC Ensembl
Innerchr6:37023884..37033752hg18UCSC Ensembl
Innerchr6:37023884..37033752hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg389869
hg199869
hg189869
hg179869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522653
Supporting Variants
Samples
Known GenesPI16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706053
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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