A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088431



Internal ID20655471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57445536..57596159hg38UCSC Ensembl
chr2:57672671..57823294hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38150624
hg19150624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088431
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