A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698358



Internal ID15435010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43417133..43450763hg38UCSC Ensembl
Innerchr19:43921285..43954915hg19UCSC Ensembl
Innerchr19:48613125..48646755hg18UCSC Ensembl
Innerchr19:48613125..48646755hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3833631
hg1933631
hg1833631
hg1733631
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520852
Supporting Variants
Samples
Known GenesTEX101
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698358
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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