A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801238



Internal ID19162744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34108410..34180899hg38UCSC Ensembl
Innerchr4:34110032..34182521hg19UCSC Ensembl
Innerchr4:33786427..33858916hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3872490
hg1972490
hg1872490
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893910
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801238
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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