A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634672



Internal ID7021475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604370..60613330hg38UCSC Ensembl
Innerchr14:60604370..60613330hg38UCSC Ensembl
Outerchr14:60604218..60613484hg38UCSC Ensembl
chr14:61071088..61080048hg19UCSC Ensembl
Innerchr14:61071088..61080048hg19UCSC Ensembl
Outerchr14:61070936..61080202hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388961
hg198961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15035859
SamplesHG01695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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