A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497704



Internal ID22555638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172653006..172663107hg38UCSC Ensembl
chr5:172080009..172090110hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3810102
hg1910102
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842126
Supporting Variants
Samples
Known GenesNEURL1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497704
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