A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257704



Internal ID20824744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202285405..202285895hg38UCSC Ensembl
chr2:203150128..203150618hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546188
Supporting Variants
Samples
Known GenesNOP58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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