A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15069085



Internal ID5070901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77135519..77138096hg38UCSC Ensembl
Innerchr14:77135524..77138092hg38UCSC Ensembl
Outerchr14:77135515..77138101hg38UCSC Ensembl
chr14:77601862..77604439hg19UCSC Ensembl
Innerchr14:77601867..77604435hg19UCSC Ensembl
Outerchr14:77601858..77604444hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382578
hg192578
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634998
Supporting Variants
SamplesNA19735
Known GenesZDHHC22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15069085
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