A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675875



Internal ID9595294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99517862..99523173hg38UCSC Ensembl
Outerchr7:99517825..99523223hg38UCSC Ensembl
Innerchr7:99115485..99120796hg19UCSC Ensembl
Outerchr7:99115448..99120846hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385399
hg195399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5816546
SamplesNA20819
Known GenesZKSCAN5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675875
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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