A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465092



Internal ID22522981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93876302..93915623hg38UCSC Ensembl
chr10:95636059..95675380hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3839322
hg1939322
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855562
Supporting Variants
Samples
Known GenesSLC35G1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465092
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