A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705241



Internal ID15095207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162587986..162610700hg38UCSC Ensembl
Innerchr6:163009018..163031732hg19UCSC Ensembl
Innerchr6:162929008..162951722hg18UCSC Ensembl
Innerchr6:162979429..163002143hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3822715
hg1922715
hg1822715
hg1722715
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)nssv705241
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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