A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635070



Internal ID6675184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80484764..80485699hg38UCSC Ensembl
Innerchr14:80484814..80485649hg38UCSC Ensembl
Outerchr14:80484683..80485780hg38UCSC Ensembl
chr14:80951107..80952042hg19UCSC Ensembl
Innerchr14:80951157..80951992hg19UCSC Ensembl
Outerchr14:80951026..80952123hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15076997, essv15076995, essv15076996, essv15076994, essv15076993, essv15076991, essv15076992
SamplesNA18881, HG03572, NA18489, HG03452, HG02144, HG03397, HG02667
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635070
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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