A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635001



Internal ID7021801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77349071..77355209hg38UCSC Ensembl
Innerchr14:77349071..77355209hg38UCSC Ensembl
Outerchr14:77348904..77355371hg38UCSC Ensembl
chr14:77815414..77821552hg19UCSC Ensembl
Innerchr14:77815414..77821552hg19UCSC Ensembl
Outerchr14:77815247..77821714hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386139
hg196139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15069089
SamplesNA19213
Known GenesTMED8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635001
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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