A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552374



Internal ID20925501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235693055..235694081hg38UCSC Ensembl
chr1:235856355..235857381hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250728
Samples
Known GenesLYST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552374
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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