A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517780



Internal ID15098387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1156508..1185028hg38UCSC Ensembl
Innerchr10:1202448..1230968hg19UCSC Ensembl
Innerchr10:1192448..1220968hg18UCSC Ensembl
Innerchr10:1192448..1220968hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3828521
hg1928521
hg1828521
hg1728521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676229, nssv653233, nssv682313, nssv696134, nssv664815, nssv688650, nssv684790
Samples
Known GenesADARB2, LINC00200
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517780
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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