A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614459



Internal ID7001353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107445487..107449278hg38UCSC Ensembl
Innerchr7:107445487..107449278hg38UCSC Ensembl
Outerchr7:107444987..107449778hg38UCSC Ensembl
chr7:107085932..107089723hg19UCSC Ensembl
Innerchr7:107085932..107089723hg19UCSC Ensembl
Outerchr7:107085432..107090223hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383792
hg193792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917708
SamplesHG01973
Known GenesCOG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614459
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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