A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660125



Internal ID15396777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36231930..36331692hg38UCSC Ensembl
Innerchr19:36722832..36822594hg19UCSC Ensembl
Innerchr19:41414672..41514434hg18UCSC Ensembl
Innerchr19:41414672..41514434hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3899763
hg1999763
hg1899763
hg1799763
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520020
Supporting Variants
Samples
Known GenesLINC00665, LOC100134317, ZNF146
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660125
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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