A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000777



Internal ID18743308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24574524..24683259hg38UCSC Ensembl
Innerchr4:24576147..24684882hg19UCSC Ensembl
Innerchr4:24185245..24293980hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38108736
hg19108736
hg18108736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5157n100
Supporting Variantsnssv3737756
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)nsv1000777
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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