A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541561



Internal ID20914843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118339791..118341130hg38UCSC Ensembl
chr1:118882414..118883753hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381340
hg191340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541561
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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