A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576696



Internal ID20949767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60437019..60437515hg38UCSC Ensembl
chr15:60729218..60729714hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241856
Samples
Known GenesNARG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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