A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635406



Internal ID7022205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95687747..95689095hg38UCSC Ensembl
Innerchr14:95687800..95689043hg38UCSC Ensembl
Outerchr14:95687695..95689148hg38UCSC Ensembl
chr14:96154084..96155432hg19UCSC Ensembl
Innerchr14:96154137..96155380hg19UCSC Ensembl
Outerchr14:96154032..96155485hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381349
hg191349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103417
SamplesNA18595
Known GenesTCL1B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635406
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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