A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669168



Internal ID9935273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75825720..75827016hg38UCSC Ensembl
Outerchr7:75825683..75827066hg38UCSC Ensembl
Innerchr7:75455038..75456334hg19UCSC Ensembl
Outerchr7:75455001..75456384hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6327965
SamplesNA18553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669168
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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