A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045593



Internal ID18788124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98564824..98588211hg38UCSC Ensembl
Innerchr10:100324581..100347968hg19UCSC Ensembl
Innerchr10:100314571..100337958hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3823388
hg1923388
hg1823388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515358
Samples
Known GenesHPSE2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045593
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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