A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596896



Internal ID6637166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87803120..87811260hg38UCSC Ensembl
Innerchr3:87803134..87811247hg38UCSC Ensembl
Outerchr3:87803107..87811274hg38UCSC Ensembl
chr3:87852270..87860410hg19UCSC Ensembl
Innerchr3:87852284..87860397hg19UCSC Ensembl
Outerchr3:87852257..87860424hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg388141
hg198141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066113, essv11066114
SamplesHG00097, HG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596896
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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