A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575258



Internal ID20948329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132686048..132686680hg38UCSC Ensembl
chr9:135561435..135562067hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280101
Samples
Known GenesGTF3C4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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