A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679045



Internal ID15415697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14805759..14808898hg38UCSC Ensembl
Innerchr19:14916571..14919710hg19UCSC Ensembl
Innerchr19:14777571..14780710hg18UCSC Ensembl
Innerchr19:14777571..14780710hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383140
hg193140
hg183140
hg173140
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517123
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679045
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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