A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077792



Internal ID20644833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149424764..149425123hg38UCSC Ensembl
chr2:150281278..150281637hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342337
Supporting Variants
Samples
Known GenesLYPD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0019


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