A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891090



Internal ID18838800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26076885..26183674hg38UCSC Ensembl
Outerchr7:26011300..26194682hg38UCSC Ensembl
Innerchr7:26116505..26223294hg19UCSC Ensembl
Outerchr7:26050920..26234302hg19UCSC Ensembl
Innerchr7:26083030..26189819hg18UCSC Ensembl
Outerchr7:26017445..26200827hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38183383
hg19183383
hg18183383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788809, essv25788355
Samples
Known GenesHNRNPA2B1, NFE2L3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891090
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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