A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678073



Internal ID15414725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56687381..56699418hg38UCSC Ensembl
Innerchr19:57198749..57210786hg19UCSC Ensembl
Innerchr19:61890561..61902598hg18UCSC Ensembl
Innerchr19:61890561..61902598hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3812038
hg1912038
hg1812038
hg1712038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517449
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678073
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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