A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653522



Internal ID15390174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35170884..35182340hg38UCSC Ensembl
Innerchr19:35661787..35673243hg19UCSC Ensembl
Innerchr19:40353627..40365083hg18UCSC Ensembl
Innerchr19:40353627..40365083hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811457
hg1911457
hg1811457
hg1711457
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516540
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653522
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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