A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257306



Internal ID20824346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230692795..230693237hg38UCSC Ensembl
chr2:231557510..231557952hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536571
Supporting Variants
Samples
Known GenesLOC151475
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257306
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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