A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10899622



Internal ID901438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2574118..2575408hg38UCSC Ensembl
Innerchr3:2574129..2575398hg38UCSC Ensembl
Outerchr3:2574108..2575419hg38UCSC Ensembl
chr3:2615802..2617092hg19UCSC Ensembl
Innerchr3:2615813..2617082hg19UCSC Ensembl
Outerchr3:2615792..2617103hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381291
hg191291
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595035
Supporting Variants
SamplesNA19819
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10899622
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