A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699508



Internal ID15089474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162467672..162499341hg38UCSC Ensembl
Innerchr6:162888704..162920373hg19UCSC Ensembl
Innerchr6:162808694..162840363hg18UCSC Ensembl
Innerchr6:162859115..162890784hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3831670
hg1931670
hg1831670
hg1731670
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)nssv699508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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