A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013961



Internal ID18756493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24574524..24690264hg38UCSC Ensembl
Innerchr4:24576147..24691887hg19UCSC Ensembl
Innerchr4:24185245..24300985hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38115741
hg19115741
hg18115741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5157n100
Supporting Variantsnssv3620594
Samples
Known GenesDHX15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013961
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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