A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660546



Internal ID15050512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161393875..161438978hg38UCSC Ensembl
Innerchr6:161814907..161860010hg19UCSC Ensembl
Innerchr6:161734897..161780000hg18UCSC Ensembl
Innerchr6:161785318..161830421hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3845104
hg1945104
hg1845104
hg1745104
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520078
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660546
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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