A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635399



Internal ID7022198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95294501..95303095hg38UCSC Ensembl
Innerchr14:95294571..95303026hg38UCSC Ensembl
Outerchr14:95294432..95303165hg38UCSC Ensembl
chr14:95760838..95769432hg19UCSC Ensembl
Innerchr14:95760908..95769363hg19UCSC Ensembl
Outerchr14:95760769..95769502hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg388595
hg198595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103387
SamplesHG01857
Known GenesCLMN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635399
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer