A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549654



Internal ID20922815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190264965..190266994hg38UCSC Ensembl
chr2:191129691..191131720hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256975
Samples
Known GenesHIBCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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