A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043468



Internal ID18785999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2237769..2343610hg38UCSC Ensembl
Innerchr10:2279963..2385804hg19UCSC Ensembl
Innerchr10:2269963..2375804hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38105842
hg19105842
hg18105842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707666
Samples
Known GenesLINC00701
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043468
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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