A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570064



Internal ID20943135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150988636..150989554hg38UCSC Ensembl
chr3:150706423..150707341hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263209
Samples
Known GenesCLRN1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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