A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665671



Internal ID9931776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74159264..74161396hg38UCSC Ensembl
Outerchr7:74159227..74161446hg38UCSC Ensembl
Innerchr7:73573594..73575726hg19UCSC Ensembl
Outerchr7:73573557..73575776hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382220
hg192220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5829244
SamplesNA19455
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665671
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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