A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047909



Internal ID19137128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42118976..42294568hg38UCSC Ensembl
Innerchr10:42614424..42790016hg19UCSC Ensembl
Innerchr10:41934430..42110022hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38175593
hg19175593
hg18175593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv716n100
Supporting Variantsnssv3707768, nssv3512500
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)nsv1047909
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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