A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539427



Internal ID20912722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99401745..99402672hg38UCSC Ensembl
chr3:99120589..99121516hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4951n223
Supporting Variantsnssv18262773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539427
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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