A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614461



Internal ID7001355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107538973..107541734hg38UCSC Ensembl
Innerchr7:107539008..107541700hg38UCSC Ensembl
Outerchr7:107538939..107541769hg38UCSC Ensembl
chr7:107179418..107182179hg19UCSC Ensembl
Innerchr7:107179453..107182145hg19UCSC Ensembl
Outerchr7:107179384..107182214hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382762
hg192762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917788
SamplesHG03755
Known GenesCOG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614461
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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