A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730126



Internal ID21400937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89213815..89214239hg38UCSC Ensembl
chr6:89923534..89923958hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256074, nssv16256622
SamplesHG00733
Known GenesGABRR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730126
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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