A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587442



Internal ID20960513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64296312..64296645hg38UCSC Ensembl
chr15:64588511..64588844hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238813
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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