A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633670



Internal ID7020478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20008774..20021351hg38UCSC Ensembl
Innerchr14:20008802..20021323hg38UCSC Ensembl
Outerchr14:20008746..20021379hg38UCSC Ensembl
chr14:20476933..20489510hg19UCSC Ensembl
Innerchr14:20476961..20489482hg19UCSC Ensembl
Outerchr14:20476905..20489538hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3812578
hg1912578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14919444
SamplesNA20531
Known GenesOR4K14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633670
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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