A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784782



Internal ID19160869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112142836..112244933hg38UCSC Ensembl
Innerchr7:111782891..111884988hg19UCSC Ensembl
Innerchr7:111570127..111672224hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38102098
hg19102098
hg18102098
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891191
Supporting Variants
Samples
Known GenesDOCK4, ZNF277
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784782
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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