A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544372



Internal ID20917612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232167343..232167834hg38UCSC Ensembl
chr1:232303089..232303580hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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