A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552612



Internal ID20925737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59021200..59021508hg38UCSC Ensembl
chr1:59486872..59487180hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552612
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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