A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012574



Internal ID18755107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:61978546..62088469hg38UCSC Ensembl
Innerchr4:62844264..62954187hg19UCSC Ensembl
Innerchr4:62526859..62636782hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38109924
hg19109924
hg18109924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626519
Samples
Known GenesLPHN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012574
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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