A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614773



Internal ID7001666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119651437..119875829hg38UCSC Ensembl
chr7:119291491..119515883hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38224393
hg19224393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12945284, essv12945286, essv12945285, essv12945283, essv12945282
SamplesHG03280, HG03133, HG02554, HG01988, NA19463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614773
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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