A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541653



Internal ID20914935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219315307..219337158hg38UCSC Ensembl
chr1:219488649..219510500hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3821852
hg1921852
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541653
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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