A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10918308



Internal ID920124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9879400..9888341hg38UCSC Ensembl
Innerchr3:9879415..9888326hg38UCSC Ensembl
Outerchr3:9879385..9888356hg38UCSC Ensembl
chr3:9921084..9930025hg19UCSC Ensembl
Innerchr3:9921099..9930010hg19UCSC Ensembl
Outerchr3:9921069..9930040hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388942
hg198942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595255
Supporting Variants
SamplesHG00449
Known GenesCIDEC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10918308
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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