A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784633



Internal ID18824970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23433673..23561605hg38UCSC Ensembl
Innerchr7:23473292..23601224hg19UCSC Ensembl
Innerchr7:23439817..23567749hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38127933
hg19127933
hg18127933
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891087
Supporting Variants
Samples
Known GenesIGF2BP3, RPS2P32, TRA2A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784633
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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