A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705769



Internal ID21378045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61571028..61571084hg38UCSC Ensembl
chr14:62037746..62037802hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391080
Supporting Variants
Samples
Known GenesFLJ22447
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705769
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.261494


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