A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516259



Internal ID15443552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62749269..62756546hg38UCSC Ensembl
Innerchr10:64509029..64516306hg19UCSC Ensembl
Innerchr10:64179035..64186312hg18UCSC Ensembl
Innerchr10:64179035..64186312hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg387278
hg197278
hg187278
hg177278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689326, nssv675622, nssv676073, nssv680930, nssv690437, nssv667136, nssv683772, nssv654636, nssv685027, nssv661316, nssv678088, nssv673597
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516259
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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