A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702999



Internal ID15092965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8150086..8206837hg38UCSC Ensembl
Innerchr19:8214970..8271721hg19UCSC Ensembl
Innerchr19:8120970..8177721hg18UCSC Ensembl
Innerchr19:8120970..8177721hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3856752
hg1956752
hg1856752
hg1756752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526669
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702999
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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