A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548050



Internal ID20878275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200886697..200887090hg38UCSC Ensembl
chr2:201751420..201751813hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256357
Samples
Known GenesPPIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548050
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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