A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267433



Internal ID20834473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160097551..160097997hg38UCSC Ensembl
chr5:159524558..159525004hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560496
Supporting Variants
Samples
Known GenesPWWP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267433
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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