A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694424



Internal ID15431076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7103531..7166098hg38UCSC Ensembl
Innerchr19:7103542..7166109hg19UCSC Ensembl
Innerchr19:7054542..7117109hg18UCSC Ensembl
Innerchr19:7054542..7117109hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3862568
hg1962568
hg1862568
hg1762568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521213
Supporting Variants
Samples
Known GenesINSR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694424
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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