A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252795



Internal ID20819835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98018909..98020278hg38UCSC Ensembl
chr1:98484465..98485834hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544493
Supporting Variants
Samples
Known GenesMIR137HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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