A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5703n100



Internal ID20157319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76783895..76838952hg38UCSC Ensembl
chr5:76079720..76134777hg19UCSC Ensembl
chr5:76115476..76170533hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3855058
hg1955058
hg1855058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018194, nsv1025151, nsv1022431, nsv1021460, nsv1031491, nsv1020397, nsv1025061, nsv1033086, nsv1015997
Samples
Known GenesF2RL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5703n100
Frequency
Sample Size29084
Observed Gain29
Observed Loss0
Observed Complex0
Frequencyn/a


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