A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797051



Internal ID19170565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83504062..83550306hg38UCSC Ensembl
Innerchr7:83133378..83179622hg19UCSC Ensembl
Innerchr7:82971314..83017558hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3846245
hg1946245
hg1846245
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891157
Supporting Variants
Samples
Known GenesSEMA3E
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797051
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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