A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635018



Internal ID7021818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77900007..77926460hg38UCSC Ensembl
Innerchr14:77900031..77926436hg38UCSC Ensembl
Outerchr14:77899983..77926484hg38UCSC Ensembl
chr14:78366350..78392803hg19UCSC Ensembl
Innerchr14:78366374..78392779hg19UCSC Ensembl
Outerchr14:78366326..78392827hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3826454
hg1926454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv410e214
Supporting Variantsessv15070081
SamplesHG01122
Known GenesADCK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635018
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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