A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579808



Internal ID20952879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41539499..41540007hg38UCSC Ensembl
chr15:41831697..41832205hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238346
Samples
Known GenesRPAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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