A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257938



Internal ID20824978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42540418..42540608hg38UCSC Ensembl
chr2:42767558..42767748hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554609
Supporting Variants
Samples
Known GenesMTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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