A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266671



Internal ID20833711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133009465..133010029hg38UCSC Ensembl
chr5:132345157..132345721hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558445
Supporting Variants
Samples
Known GenesZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266671
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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