A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698654



Internal ID15435306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8985576..8990996hg38UCSC Ensembl
Innerchr19:9096252..9101672hg19UCSC Ensembl
Innerchr19:8957252..8962672hg18UCSC Ensembl
Innerchr19:8957252..8962672hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385421
hg195421
hg185421
hg175421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522984
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698654
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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