A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575672



Internal ID20948743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22645399..22645911hg38UCSC Ensembl
chr10:22934328..22934840hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224310
Samples
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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