A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257016



Internal ID21398284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76109065..76158338hg38UCSC Ensembl
chr6:76818782..76868055hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3849274
hg1949274
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730199
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257016
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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