A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695103



Internal ID15085069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43302407..43331618hg38UCSC Ensembl
Innerchr19:43806559..43835770hg19UCSC Ensembl
Innerchr19:48498399..48527610hg18UCSC Ensembl
Innerchr19:48498399..48527610hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3829212
hg1929212
hg1829212
hg1729212
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695103
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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