A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042079



Internal ID18784610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73926463..74086173hg38UCSC Ensembl
Innerchr10:75686221..75845931hg19UCSC Ensembl
Innerchr10:75356227..75515937hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38159711
hg19159711
hg18159711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv924n100
Supporting Variantsnssv3508967
Samples
Known GenesVCL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042079
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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