A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705016



Internal ID15094982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162214013..162221692hg38UCSC Ensembl
Innerchr6:162635045..162642724hg19UCSC Ensembl
Innerchr6:162555035..162562714hg18UCSC Ensembl
Innerchr6:162605456..162613135hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg387680
hg197680
hg187680
hg177680
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)nssv705016
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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