A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577890



Internal ID20950961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64085724..64086300hg38UCSC Ensembl
chr15:64377923..64378499hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238800
Samples
Known GenesFAM96A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577890
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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