A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634677



Internal ID6674794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60897179..60930390hg38UCSC Ensembl
Innerchr14:60897179..60930390hg38UCSC Ensembl
Outerchr14:60896679..60930890hg38UCSC Ensembl
chr14:61363897..61397108hg19UCSC Ensembl
Innerchr14:61363897..61397108hg19UCSC Ensembl
Outerchr14:61363397..61397608hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3833212
hg1933212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15035932
SamplesNA20785
Known GenesMNAT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634677
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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