A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248002



Internal ID20815042
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 StatusS
Merged Variantsnsv6548574
Supporting Variants
Samples
Known GenesALDH9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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