A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578192



Internal ID20951263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78118460..78119607hg38UCSC Ensembl
chr15:78410802..78411949hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239718
Samples
Known GenesCIB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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