A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607808



Internal ID6994739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181082434..181114750hg38UCSC Ensembl
Innerchr5:181082441..181114744hg38UCSC Ensembl
Outerchr5:181082428..181114757hg38UCSC Ensembl
chr5:180509434..180541750hg19UCSC Ensembl
Innerchr5:180509441..180541744hg19UCSC Ensembl
Outerchr5:180509428..180541757hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3832317
hg1932317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12156256
SamplesHG04152
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607808
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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