A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239575



Internal ID20806615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43811372..43811903hg38UCSC Ensembl
chr15:44103570..44104101hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583613
Supporting Variants
Samples
Known GenesMFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239575
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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