A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14926096



Internal ID3103384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21203634..21204509hg38UCSC Ensembl
Innerchr14:21203635..21204508hg38UCSC Ensembl
Outerchr14:21203633..21204510hg38UCSC Ensembl
chr14:21671793..21672668hg19UCSC Ensembl
Innerchr14:21671794..21672667hg19UCSC Ensembl
Outerchr14:21671792..21672669hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633706
Supporting Variants
SamplesHG02725
Known GenesLINC00641
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14926096
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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