A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041684



Internal ID19130903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5680336hg38UCSC Ensembl
Innerchr10:5665458..5722299hg19UCSC Ensembl
Innerchr10:5705464..5762305hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3856842
hg1956842
hg1856842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv665n100
Supporting Variantsnssv3488643
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)nsv1041684
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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