A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698459



Internal ID15435111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100092820..100114484hg38UCSC Ensembl
Innerchr6:100540696..100562360hg19UCSC Ensembl
Innerchr6:100647417..100669081hg18UCSC Ensembl
Innerchr6:100647417..100669081hg17UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3821665
hg1921665
hg1821665
hg1721665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522813
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698459
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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