A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571324



Internal ID20944395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96362337..96363145hg38UCSC Ensembl
chr9:99124619..99125427hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281548
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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