A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15035859



Internal ID1819839
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634672
Supporting Variants
SamplesHG01695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15035859
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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