A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635345



Internal ID7022144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92850932..92852615hg38UCSC Ensembl
Innerchr14:92850958..92852589hg38UCSC Ensembl
Outerchr14:92850906..92852641hg38UCSC Ensembl
chr14:93317277..93318960hg19UCSC Ensembl
Innerchr14:93317303..93318934hg19UCSC Ensembl
Outerchr14:93317251..93318986hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15098112, essv15098110, essv15098108, essv15098103, essv15098105, essv15098104, essv15098102, essv15098111, essv15098106, essv15098107, essv15098109
SamplesHG03009, HG03788, HG04029, HG03902, NA21118, HG04177, NA20876, HG04054, HG03894, NA21104, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635345
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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