A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544763



Internal ID20918000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25177269..25178099hg38UCSC Ensembl
chr1:25503760..25504590hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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