A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258299



Internal ID20825339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61270751..61271086hg38UCSC Ensembl
chr2:61497886..61498221hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536152
Supporting Variants
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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