A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496377



Internal ID22554311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156449093..156454931hg38UCSC Ensembl
chr5:155876103..155881941hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385839
hg195839
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842070
Supporting Variants
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496377
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