A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613551



Internal ID7000447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67470559..67476394hg38UCSC Ensembl
Innerchr7:67470572..67476382hg38UCSC Ensembl
Outerchr7:67470547..67476407hg38UCSC Ensembl
chr7:66935546..66941381hg19UCSC Ensembl
Innerchr7:66935559..66941369hg19UCSC Ensembl
Outerchr7:66935534..66941394hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12826496
SamplesHG04107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613551
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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