A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574775



Internal ID20947846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112937483..112939601hg38UCSC Ensembl
chr3:112656330..112658448hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259224
Samples
Known GenesCD200R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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