A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042955



Internal ID18785486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86479594..86585847hg38UCSC Ensembl
Innerchr10:88239351..88345604hg19UCSC Ensembl
Innerchr10:88229331..88335584hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38106254
hg19106254
hg18106254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv947n100
Supporting Variantsnssv3514604
Samples
Known GenesWAPAL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042955
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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