A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891087



Internal ID19185483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23433673..23561605hg38UCSC Ensembl
Outerchr7:23433673..23561605hg38UCSC Ensembl
Innerchr7:23473292..23601224hg19UCSC Ensembl
Outerchr7:23473292..23601224hg19UCSC Ensembl
Innerchr7:23439817..23567749hg18UCSC Ensembl
Outerchr7:23439817..23567749hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38127933
hg19127933
hg18127933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784633, essv25783855
Samples
Known GenesIGF2BP3, RPS2P32, TRA2A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891087
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer