A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654696



Internal ID15391348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19749714..19755562hg38UCSC Ensembl
Innerchr19:19860523..19866371hg19UCSC Ensembl
Innerchr19:19721523..19727371hg18UCSC Ensembl
Innerchr19:19721523..19727371hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385849
hg195849
hg185849
hg175849
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517362
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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