A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578003



Internal ID20951074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40637781..40638749hg38UCSC Ensembl
chr15:40929979..40930947hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2503n223
Supporting Variantsnssv18238262
Samples
Known GenesCASC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578003
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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