A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695884



Internal ID15432536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32779985..32824007hg38UCSC Ensembl
Innerchr19:33270891..33314913hg19UCSC Ensembl
Innerchr19:37962731..38006753hg18UCSC Ensembl
Innerchr19:37962731..38006753hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3844023
hg1944023
hg1844023
hg1744023
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518446
Supporting Variants
Samples
Known GenesTDRD12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695884
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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