A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614269



Internal ID7001164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99079962..99082643hg38UCSC Ensembl
Innerchr7:99079964..99082642hg38UCSC Ensembl
Outerchr7:99079961..99082645hg38UCSC Ensembl
chr7:98677585..98680266hg19UCSC Ensembl
Innerchr7:98677587..98680265hg19UCSC Ensembl
Outerchr7:98677584..98680268hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382682
hg192682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12906235
SamplesHG03681
Known GenesSMURF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614269
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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