A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077786



Internal ID20644827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149209042..149209670hg38UCSC Ensembl
chr2:150065556..150066184hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352124
Supporting Variants
Samples
Known GenesLYPD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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