A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542763



Internal ID20916015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157391203..157400396hg38UCSC Ensembl
chr1:157360993..157370186hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389194
hg199194
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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