A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041462



Internal ID19130681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87758972..87824527hg38UCSC Ensembl
Innerchr10:89518729..89584284hg19UCSC Ensembl
Innerchr10:89508709..89574264hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3865556
hg1965556
hg1865556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511966
Samples
Known GenesATAD1, CFL1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041462
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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