A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250094



Internal ID20817134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24005797..24006513hg38UCSC Ensembl
chr1:24332287..24333003hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250094
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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