A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605690



Internal ID6992628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85807095..85812417hg38UCSC Ensembl
Innerchr5:85807096..85812416hg38UCSC Ensembl
Outerchr5:85807094..85812418hg38UCSC Ensembl
chr5:85102913..85108235hg19UCSC Ensembl
Innerchr5:85102914..85108234hg19UCSC Ensembl
Outerchr5:85102912..85108236hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385323
hg195323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11964889
SamplesHG00273
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605690
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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