A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5495n100



Internal ID20157111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186554708..186992197hg38UCSC Ensembl
chr4:187475862..187913351hg19UCSC Ensembl
chr4:187712856..188150345hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38437490
hg19437490
hg18437490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026970, nsv1022262
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)dgv5495n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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