A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635442



Internal ID7022241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97419131..97423595hg38UCSC Ensembl
Innerchr14:97419131..97423595hg38UCSC Ensembl
Outerchr14:97419104..97423763hg38UCSC Ensembl
chr14:97885468..97889932hg19UCSC Ensembl
Innerchr14:97885468..97889932hg19UCSC Ensembl
Outerchr14:97885441..97890100hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384465
hg194465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103712
SamplesNA12717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635442
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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