A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540603



Internal ID20913892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23832500..23833407hg38UCSC Ensembl
chr1:24158990..24159897hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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