A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797317



Internal ID19160390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111275283..111585090hg38UCSC Ensembl
Innerchr7:110915339..111225146hg19UCSC Ensembl
Innerchr7:110702575..111012382hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38309808
hg19309808
hg18309808
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891183
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797317
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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