A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257443



Internal ID20824483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238798778..238799046hg38UCSC Ensembl
chr2:239707419..239707687hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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