A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634090



Internal ID7020894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37601792..37606824hg38UCSC Ensembl
Innerchr14:37601792..37606824hg38UCSC Ensembl
Outerchr14:37601657..37606892hg38UCSC Ensembl
chr14:38070997..38076029hg19UCSC Ensembl
Innerchr14:38070997..38076029hg19UCSC Ensembl
Outerchr14:38070862..38076097hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg385033
hg195033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14969954, essv14969955, essv14969953
SamplesNA18977, NA19036, HG01747
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634090
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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