A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664810



Internal ID15054776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162493954..162541230hg38UCSC Ensembl
Innerchr6:162914986..162962262hg19UCSC Ensembl
Innerchr6:162834976..162882252hg18UCSC Ensembl
Innerchr6:162885397..162932673hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3847277
hg1947277
hg1847277
hg1747277
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)nssv664810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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