A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039748



Internal ID19128967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42154929..42294568hg38UCSC Ensembl
Innerchr10:42650377..42790016hg19UCSC Ensembl
Innerchr10:41970383..42110022hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38139640
hg19139640
hg18139640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv716n100
Supporting Variantsnssv3509498
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039748
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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