A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548574



Internal ID20921757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165694936..165695488hg38UCSC Ensembl
chr1:165664173..165664725hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248002
Samples
Known GenesALDH9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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