A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267037



Internal ID20834077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71595022..71595429hg38UCSC Ensembl
chr5:70890849..70891256hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555596
Supporting Variants
Samples
Known GenesMCCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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