A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256992



Internal ID20824032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190885951..190886832hg38UCSC Ensembl
chr2:191750677..191751558hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545401
Supporting Variants
Samples
Known GenesGLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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