A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552181



Internal ID20925309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177618184..177619949hg38UCSC Ensembl
chr1:177587319..177589084hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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