A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542974



Internal ID20916225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150916816..150918934hg38UCSC Ensembl
chr1:150889292..150891410hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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