A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614252



Internal ID7001147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98225004..98236964hg38UCSC Ensembl
Innerchr7:98225004..98236964hg38UCSC Ensembl
Outerchr7:98224818..98237131hg38UCSC Ensembl
chr7:97854316..97866276hg19UCSC Ensembl
Innerchr7:97854316..97866276hg19UCSC Ensembl
Outerchr7:97854130..97866443hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811961
hg1911961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12905056, essv12905055
SamplesNA19917, HG01926
Known GenesTECPR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614252
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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