A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251927



Internal ID20818967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87639733..87640288hg38UCSC Ensembl
chr1:88105416..88105971hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251927
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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