A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697596



Internal ID15087562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74588374..74612279hg38UCSC Ensembl
Innerchr10:76348132..76372037hg19UCSC Ensembl
Innerchr10:76018138..76042043hg18UCSC Ensembl
Innerchr10:76018138..76042043hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3823906
hg1923906
hg1823906
hg1723906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515824
Supporting Variants
Samples
Known GenesADK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697596
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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