A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548265



Internal ID20921457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145717994..145718743hg38UCSC Ensembl
chr2:146475562..146476311hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548265
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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