A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10899560



Internal ID901376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2304094..2362716hg38UCSC Ensembl
Innerchr3:2304594..2362216hg38UCSC Ensembl
Outerchr3:2303094..2363716hg38UCSC Ensembl
chr3:2345778..2404400hg19UCSC Ensembl
Innerchr3:2346278..2403900hg19UCSC Ensembl
Outerchr3:2344778..2405400hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3858623
hg1958623
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595025
Supporting Variants
SamplesNA18873
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10899560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer