A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635307



Internal ID6675420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90175817..90176850hg38UCSC Ensembl
Innerchr14:90175827..90176840hg38UCSC Ensembl
Outerchr14:90175807..90176860hg38UCSC Ensembl
chr14:90642161..90643194hg19UCSC Ensembl
Innerchr14:90642171..90643184hg19UCSC Ensembl
Outerchr14:90642151..90643204hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093255
SamplesHG02085
Known GenesKCNK13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635307
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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