A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579675



Internal ID20952746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73457669..73458421hg38UCSC Ensembl
chr10:75217427..75218179hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235734
Samples
Known GenesPPP3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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