A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635271



Internal ID7022070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88122875..88123781hg38UCSC Ensembl
Innerchr14:88122930..88123726hg38UCSC Ensembl
Outerchr14:88122820..88123836hg38UCSC Ensembl
chr14:88589219..88590125hg19UCSC Ensembl
Innerchr14:88589274..88590070hg19UCSC Ensembl
Outerchr14:88589164..88590180hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15092279
SamplesHG00119
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635271
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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