A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658973



Internal ID15048939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29974289..30055277hg38UCSC Ensembl
Innerchr19:30465196..30546184hg19UCSC Ensembl
Innerchr19:35157036..35238024hg18UCSC Ensembl
Innerchr19:35157036..35238024hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3880989
hg1980989
hg1880989
hg1780989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519832
Supporting Variants
Samples
Known GenesURI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658973
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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