A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021256



Internal ID20588296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70479733..70504233hg38UCSC Ensembl
chr14:70946450..70970950hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3824501
hg1924501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475703
Supporting Variants
Samples
Known GenesADAM20P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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