A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257330



Internal ID20824370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231492127..231492325hg38UCSC Ensembl
chr2:232356838..232357036hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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