A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667525



Internal ID15057491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4875696..4878596hg38UCSC Ensembl
Innerchr19:4875708..4878608hg19UCSC Ensembl
Innerchr19:4826708..4829608hg18UCSC Ensembl
Innerchr19:4826708..4829608hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382901
hg192901
hg182901
hg172901
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517448
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667525
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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