A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075718



Internal ID20642758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:115475501..115478600hg38UCSC Ensembl
chr2:116233077..116236176hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351181
Supporting Variants
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075718
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