A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11260536



Internal ID5228201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187206126..187210140hg38UCSC Ensembl
Innerchr3:187206165..187210102hg38UCSC Ensembl
Outerchr3:187206088..187210179hg38UCSC Ensembl
chr3:186923914..186927928hg19UCSC Ensembl
Innerchr3:186923953..186927890hg19UCSC Ensembl
Outerchr3:186923876..186927967hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg384015
hg194015
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599006
Supporting Variants
SamplesNA18625
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11260536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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