A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552644



Internal ID20925770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170546313..170546786hg38UCSC Ensembl
chr1:170515454..170515927hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248079
Samples
Known GenesGORAB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552644
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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