A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256532



Internal ID21399186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108246446..108460614hg38UCSC Ensembl
chr1:108789068..109003236hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38214169
hg19214169
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730086
Supporting Variants
SamplesHG00732
Known GenesNBPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256532
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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