A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490894



Internal ID22548818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2099276..2102894hg38UCSC Ensembl
chr3:2140960..2144578hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383619
hg193619
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835538
Supporting Variants
Samples
Known GenesCNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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