A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585802



Internal ID20958873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64290827..64291493hg38UCSC Ensembl
chr15:64583026..64583692hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2564n223
Supporting Variantsnssv18238811
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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