A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538642



Internal ID20911956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67634392..67638166hg38UCSC Ensembl
chr1:68100075..68103849hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383775
hg193775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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