A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256074



Internal ID21399696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89213815..89214232hg38UCSC Ensembl
chr6:89923534..89923951hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730126
Supporting Variants
SamplesHG00733
Known GenesGABRR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256074
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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