A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039290



Internal ID18781821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15537021..15664910hg38UCSC Ensembl
Innerchr10:15579020..15706909hg19UCSC Ensembl
Innerchr10:15619026..15746915hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38127890
hg19127890
hg18127890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv679n100
Supporting Variantsnssv3505782
Samples
Known GenesITGA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039290
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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