A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251830



Internal ID20818870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44155626..44157235hg38UCSC Ensembl
chr1:44621298..44622907hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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