A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581004



Internal ID20954075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34142723..34143250hg38UCSC Ensembl
chr15:34434924..34435451hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239540
Samples
Known GenesKATNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer