A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557051



Internal ID20930122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121457669..121458055hg38UCSC Ensembl
chr9:124219947..124220333hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279764
Samples
Known GenesGGTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557051
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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