A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579845



Internal ID20952916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42428825..42429314hg38UCSC Ensembl
chr15:42721023..42721512hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238999
Samples
Known GenesZNF106
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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