A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797528



Internal ID19180263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:57643357..57678808hg38UCSC Ensembl
Innerchr5:56939184..56974635hg19UCSC Ensembl
Innerchr5:56974941..57010392hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3835452
hg1935452
hg1835452
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894193
Supporting Variants
Samples
Known GenesLOC101928505
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797528
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer