A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696766



Internal ID15433418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54245159..54247206hg38UCSC Ensembl
Innerchr19:54749011..54751065hg19UCSC Ensembl
Innerchr19:59440823..59442877hg18UCSC Ensembl
Innerchr19:59440823..59442877hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382048
hg192055
hg182055
hg172055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517129
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696766
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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