A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257733



Internal ID20824773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202455910..202456205hg38UCSC Ensembl
chr2:203320633..203320928hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553681
Supporting Variants
Samples
Known GenesBMPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257733
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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