A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696397



Internal ID15086363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161372287..161985303hg38UCSC Ensembl
Innerchr6:161793319..162406335hg19UCSC Ensembl
Innerchr6:161713309..162326325hg18UCSC Ensembl
Innerchr6:161763730..162376746hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38613017
hg19613017
hg18613017
hg17613017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518931
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696397
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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