A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256240



Internal ID21398332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76108871..76159264hg38UCSC Ensembl
chr6:76818588..76868981hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3850394
hg1950394
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)nssv16256240
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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