A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583574



Internal ID20956645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82562557..82563482hg38UCSC Ensembl
chr15:83231307..83232232hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240411
Samples
Known GenesCPEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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