A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256364



Internal ID20823404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200970733..200971193hg38UCSC Ensembl
chr2:201835456..201835916hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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