A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699597



Internal ID15089563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162368165..162624431hg38UCSC Ensembl
Innerchr6:162789197..163045463hg19UCSC Ensembl
Innerchr6:162709187..162965453hg18UCSC Ensembl
Innerchr6:162759608..163015874hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38256267
hg19256267
hg18256267
hg17256267
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699597
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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