A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052417



Internal ID19141636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42118976..42332543hg38UCSC Ensembl
Innerchr10:42614424..42827991hg19UCSC Ensembl
Innerchr10:41934430..42147997hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38213568
hg19213568
hg18213568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv717n100
Supporting Variantsnssv3519245
Samples
Known GenesLOC441666
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052417
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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