A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038690



Internal ID19127909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5678461hg38UCSC Ensembl
Innerchr10:5665458..5720424hg19UCSC Ensembl
Innerchr10:5705464..5760430hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3854967
hg1954967
hg1854967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv665n100
Supporting Variantsnssv3485935
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)nsv1038690
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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