A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257797



Internal ID20824837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203110467..203110988hg38UCSC Ensembl
chr2:203975190..203975711hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537800
Supporting Variants
Samples
Known GenesNBEAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257797
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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