A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022262



Internal ID18764796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186554708..186927130hg38UCSC Ensembl
Innerchr4:187475862..187848284hg19UCSC Ensembl
Innerchr4:187712856..188085278hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38372423
hg19372423
hg18372423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5495n100
Supporting Variantsnssv3744535
Samples
Known GenesFAT1, MTNR1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022262
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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