A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976811



Internal ID51926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177496560..177496700hg38UCSC Ensembl
chr5:176923561..176923701hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559468
Supporting Variants
Samples
Known GenesPDLIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976811
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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