A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701108



Internal ID15091074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162442446..162457662hg38UCSC Ensembl
Innerchr6:162863478..162878694hg19UCSC Ensembl
Innerchr6:162783468..162798684hg18UCSC Ensembl
Innerchr6:162833889..162849105hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3815217
hg1915217
hg1815217
hg1715217
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)nssv701108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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