A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516968



Internal ID15097575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133239517..133275531hg38UCSC Ensembl
Innerchr10:135053021..135089035hg19UCSC Ensembl
Innerchr10:134903011..134939025hg18UCSC Ensembl
Innerchr10:134941902..134977916hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3836015
hg1936015
hg1836015
hg1736015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692927, nssv666847, nssv679839, nssv689838, nssv661060, nssv696897, nssv658118, nssv696636
Samples
Known GenesADAM8, MIR202, MIR202HG, VENTX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516968
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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