A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043251



Internal ID19132470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5674592hg38UCSC Ensembl
Innerchr10:5665458..5716555hg19UCSC Ensembl
Innerchr10:5705464..5756561hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851098
hg1951098
hg1851098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv665n100
Supporting Variantsnssv3494522, nssv3483874
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043251
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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