A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11791172



Internal ID1271903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3572271..3589595hg38UCSC Ensembl
Innerchr5:3572298..3589569hg38UCSC Ensembl
Outerchr5:3572245..3589622hg38UCSC Ensembl
chr5:3572385..3589709hg19UCSC Ensembl
Innerchr5:3572412..3589683hg19UCSC Ensembl
Outerchr5:3572359..3589736hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3817325
hg1917325
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603858
Supporting Variants
SamplesHG01121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11791172
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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