A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584314



Internal ID20957385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45596429..45597340hg38UCSC Ensembl
chr15:45888627..45889538hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38912
hg19912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240307
Samples
Known GenesBLOC1S6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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