A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667887



Internal ID9933992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148910285..148937776hg38UCSC Ensembl
Outerchr7:148910248..148937826hg38UCSC Ensembl
Innerchr7:148607377..148634868hg19UCSC Ensembl
Outerchr7:148607340..148634918hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3827579
hg1927579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6353108
SamplesHG01516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667887
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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