A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697286



Internal ID15087252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162344057..162354823hg38UCSC Ensembl
Innerchr6:162765089..162775855hg19UCSC Ensembl
Innerchr6:162685079..162695845hg18UCSC Ensembl
Innerchr6:162735500..162746266hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3810767
hg1910767
hg1810767
hg1710767
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)nssv697286
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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