A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551368



Internal ID20924504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5523724..5524933hg38UCSC Ensembl
chr1:5583784..5584993hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551368
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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