A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249839



Internal ID20816879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56689557..56690275hg38UCSC Ensembl
chr1:57155230..57155948hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555113
Supporting Variants
Samples
Known GenesPRKAA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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