A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607672



Internal ID6994604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176510921..176516856hg38UCSC Ensembl
Innerchr5:176511421..176516356hg38UCSC Ensembl
Outerchr5:176509921..176517856hg38UCSC Ensembl
chr5:175937922..175943857hg19UCSC Ensembl
Innerchr5:175938422..175943357hg19UCSC Ensembl
Outerchr5:175936922..175944857hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg385936
hg195936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12142299
SamplesHG04198
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer