A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654165



Internal ID15044131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162317673..162318733hg38UCSC Ensembl
Innerchr6:162738705..162739765hg19UCSC Ensembl
Innerchr6:162658695..162659755hg18UCSC Ensembl
Innerchr6:162709116..162710176hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381061
hg191061
hg181061
hg171061
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)nssv654165
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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