A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675421



Internal ID15065387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162163721..162171775hg38UCSC Ensembl
Innerchr6:162584753..162592807hg19UCSC Ensembl
Innerchr6:162504743..162512797hg18UCSC Ensembl
Innerchr6:162555164..162563218hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg388055
hg198055
hg188055
hg178055
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)nssv675421
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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