A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656846



Internal ID9922951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13232472..13273376hg38UCSC Ensembl
Outerchr7:13232315..13273529hg38UCSC Ensembl
Innerchr7:13272097..13313001hg19UCSC Ensembl
Outerchr7:13271940..13313154hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3841215
hg1941215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5713017, essv5481346
SamplesHG00635, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656846
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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