A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614265



Internal ID7001160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98999684..99016092hg38UCSC Ensembl
Innerchr7:98999684..99016092hg38UCSC Ensembl
Outerchr7:98999184..99016592hg38UCSC Ensembl
chr7:98597307..98613715hg19UCSC Ensembl
Innerchr7:98597307..98613715hg19UCSC Ensembl
Outerchr7:98596807..98614215hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3816409
hg1916409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12906230, essv12906231, essv12906229
SamplesNA19908, HG00629, HG00266
Known GenesTRRAP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614265
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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