A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549159



Internal ID20922327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182978989..182979276hg38UCSC Ensembl
chr1:182948124..182948411hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549159
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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