A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706114



Internal ID15096080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44376201..44385498hg38UCSC Ensembl
Innerchr19:44880360..44889660hg19UCSC Ensembl
Innerchr19:49572200..49581500hg18UCSC Ensembl
Innerchr19:49572200..49581500hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg389298
hg199301
hg189301
hg179301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515911
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706114
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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