A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519430



Internal ID15446723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19815811..19822598hg38UCSC Ensembl
Innerchr7:19855434..19862221hg19UCSC Ensembl
Innerchr7:19821959..19828746hg18UCSC Ensembl
Innerchr7:19628674..19635461hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386788
hg196788
hg186788
hg176788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656176, nssv691319
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519430
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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