A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516576



Internal ID15443869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7582823..7590924hg38UCSC Ensembl
Innerchr19:7647709..7655810hg19UCSC Ensembl
Innerchr19:7553709..7561810hg18UCSC Ensembl
Innerchr19:7553709..7561810hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388102
hg198102
hg188102
hg178102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669276, nssv673996, nssv692427, nssv657478
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516576
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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