A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519428



Internal ID15446721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7997936..8039781hg38UCSC Ensembl
Innerchr9:7997936..8039781hg19UCSC Ensembl
Innerchr9:7987936..8029781hg18UCSC Ensembl
Innerchr9:7987936..8029781hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841846
hg1941846
hg1841846
hg1741846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688980, nssv656685, nssv656956, nssv673151, nssv695847, nssv679180, nssv672840, nssv656155, nssv681110, nssv684516, nssv677417
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519428
Frequency
Sample Size2026
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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