A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659850



Internal ID9579269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26182419..26183062hg38UCSC Ensembl
Outerchr7:26182262..26183215hg38UCSC Ensembl
Innerchr7:26222039..26222682hg19UCSC Ensembl
Outerchr7:26221882..26222835hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5665914, essv6413572, essv5817629, essv6003083
SamplesNA18627, HG00543, NA18541, NA18549
Known GenesNFE2L3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659850
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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