A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191889



Internal ID511569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155738764..155751063hg38UCSC Ensembl
Innerchr3:155738764..155751063hg38UCSC Ensembl
Outerchr3:155738264..155751563hg38UCSC Ensembl
chr3:155456553..155468852hg19UCSC Ensembl
Innerchr3:155456553..155468852hg19UCSC Ensembl
Outerchr3:155456053..155469352hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3812300
hg1912300
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598282
Supporting Variants
SamplesHG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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