A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635544



Internal ID7022343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102156030..102164201hg38UCSC Ensembl
Innerchr14:102156030..102164201hg38UCSC Ensembl
Outerchr14:102155849..102164383hg38UCSC Ensembl
chr14:102622367..102630538hg19UCSC Ensembl
Innerchr14:102622367..102630538hg19UCSC Ensembl
Outerchr14:102622186..102630720hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg388172
hg198172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109345, essv15109346, essv15109347, essv15109344
SamplesNA19700, NA19397, HG03449, NA19376
Known GenesWDR20
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635544
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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