A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191736



Internal ID931700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155402694..155407015hg38UCSC Ensembl
Innerchr3:155402694..155407015hg38UCSC Ensembl
Outerchr3:155402402..155407250hg38UCSC Ensembl
chr3:155120483..155124804hg19UCSC Ensembl
Innerchr3:155120483..155124804hg19UCSC Ensembl
Outerchr3:155120191..155125039hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384322
hg194322
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598276
Supporting Variants
SamplesHG00556
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191736
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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