A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976530



Internal ID51744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164537844..164548601hg38UCSC Ensembl
chr5:163964850..163975607hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3810758
hg1910758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147196
Supporting Variants
Samples
Known GenesLOC102546299
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976530
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001874


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