A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788355



Internal ID18824202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26011300..26194682hg38UCSC Ensembl
Innerchr7:26050920..26234302hg19UCSC Ensembl
Innerchr7:26017445..26200827hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38183383
hg19183383
hg18183383
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891090
Supporting Variants
Samples
Known GenesHNRNPA2B1, NFE2L3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=33
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788355
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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