A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039685



Internal ID19128904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19646166..19750692hg38UCSC Ensembl
Innerchr10:19935095..20039621hg19UCSC Ensembl
Innerchr10:19975101..20079627hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38104527
hg19104527
hg18104527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707704
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)nsv1039685
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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