A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041270



Internal ID18783801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73926463..74076624hg38UCSC Ensembl
Innerchr10:75686221..75836382hg19UCSC Ensembl
Innerchr10:75356227..75506388hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38150162
hg19150162
hg18150162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv924n100
Supporting Variantsnssv3511042
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)nsv1041270
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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