A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653175



Internal ID15043141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162163721..162165034hg38UCSC Ensembl
Innerchr6:162584753..162586066hg19UCSC Ensembl
Innerchr6:162504743..162506056hg18UCSC Ensembl
Innerchr6:162555164..162556477hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381314
hg191314
hg181314
hg171314
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)nssv653175
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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