A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270236



Internal ID20837276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76865931..76866182hg38UCSC Ensembl
chr5:76161756..76162007hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560641
Supporting Variants
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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