A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575359



Internal ID20948430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181653332..181654009hg38UCSC Ensembl
chr3:181371120..181371797hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261201
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575359
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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