A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257317



Internal ID20824357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231199884..231200523hg38UCSC Ensembl
chr2:232064598..232065237hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540728
Supporting Variants
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257317
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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