A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796132



Internal ID19164388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20438825..20496241hg38UCSC Ensembl
Innerchr7:20478448..20535864hg19UCSC Ensembl
Innerchr7:20444973..20502389hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3857417
hg1957417
hg1857417
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891085
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796132
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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