A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797739



Internal ID19166957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40154660..40215523hg38UCSC Ensembl
Innerchr7:40194259..40255122hg19UCSC Ensembl
Innerchr7:40160784..40221647hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3860864
hg1960864
hg1860864
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891100
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797739
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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