A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045910



Internal ID18788441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2068216..2351801hg38UCSC Ensembl
Innerchr10:2110410..2393995hg19UCSC Ensembl
Innerchr10:2100410..2383995hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38283586
hg19283586
hg18283586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3490646
Samples
Known GenesLINC00701, MIR6072
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045910
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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