A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565241



Internal ID20938312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136587277..136588562hg38UCSC Ensembl
chr3:136306119..136307404hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381286
hg191286
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260338
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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