A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014571



Internal ID18757106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14156596..14197243hg38UCSC Ensembl
Innerchr3:14198096..14238743hg19UCSC Ensembl
Innerchr3:14173098..14213747hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3840648
hg1940648
hg1840650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593085
Samples
Known GenesLSM3, XPC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014571
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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