A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257433



Internal ID20824473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238070470..238071086hg38UCSC Ensembl
chr2:238979111..238979727hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540450
Supporting Variants
Samples
Known GenesSCLY, UBE2F-SCLY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257433
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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