A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257812



Internal ID20824852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20323884..20324009hg38UCSC Ensembl
chr2:20523645..20523770hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554950
Supporting Variants
Samples
Known GenesPUM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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