A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3484259



Internal ID19071900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5607797..5675162hg38UCSC Ensembl
Innerchr10:5649760..5717125hg19UCSC Ensembl
Innerchr10:5689766..5757131hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3867366
hg1967366
hg1867366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050965
Supporting Variants
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)nssv3484259
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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