A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543318



Internal ID21867673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100387810..100563731hg38UCSC Ensembl
chr5:99723514..99899435hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38175922
hg19175922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107040
Supporting Variants
Samples
Known GenesFAM174A, LOC100133050
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543318
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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