A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052477



Internal ID19141696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21521341..21600797hg38UCSC Ensembl
Innerchr10:21810270..21889726hg19UCSC Ensembl
Innerchr10:21850276..21929732hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3879457
hg1979457
hg1879457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707717, nssv3707716
Samples
Known GenesMLLT10, SKIDA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052477
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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