A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779416



Internal ID19170175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115749506..115784711hg38UCSC Ensembl
Innerchr5:115085203..115120408hg19UCSC Ensembl
Innerchr5:115113102..115148307hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3835206
hg1935206
hg1835206
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890717
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779416
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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