A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517484



Internal ID15444777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10614388..10617442hg38UCSC Ensembl
Innerchr10:10656351..10659405hg19UCSC Ensembl
Innerchr10:10696357..10699411hg18UCSC Ensembl
Innerchr10:10696357..10699411hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383055
hg193055
hg183055
hg173055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652161, nssv693928, nssv682480, nssv652422, nssv685024, nssv674294
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517484
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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