A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040932



Internal ID19130151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5595907..5623811hg38UCSC Ensembl
Innerchr10:5637870..5665774hg19UCSC Ensembl
Innerchr10:5677876..5705780hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3827905
hg1927905
hg1827905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486649
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)nsv1040932
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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