A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003486



Internal ID18746017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188157145..188284087hg38UCSC Ensembl
Innerchr3:187874933..188001875hg19UCSC Ensembl
Innerchr3:189357627..189484569hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38126943
hg19126943
hg18126943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615040
Samples
Known GenesFLJ42393, LPP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003486
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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