A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613865



Internal ID6654073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80668550..80670502hg38UCSC Ensembl
Innerchr7:80668562..80670491hg38UCSC Ensembl
Outerchr7:80668539..80670514hg38UCSC Ensembl
chr7:80297866..80299818hg19UCSC Ensembl
Innerchr7:80297878..80299807hg19UCSC Ensembl
Outerchr7:80297855..80299830hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381953
hg191953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12861266
SamplesHG02660
Known GenesCD36
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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