A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635622



Internal ID7022421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104523968..104535758hg38UCSC Ensembl
Innerchr14:104523991..104535735hg38UCSC Ensembl
Outerchr14:104523945..104535781hg38UCSC Ensembl
chr14:104990305..105002095hg19UCSC Ensembl
Innerchr14:104990328..105002072hg19UCSC Ensembl
Outerchr14:104990282..105002118hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3811791
hg1911791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15114736
SamplesHG02836
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635622
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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