A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258747



Internal ID21398821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108241201..108460618hg38UCSC Ensembl
chr1:108783823..109003240hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38219418
hg19219418
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730086
Supporting Variants
SamplesHG00731
Known GenesNBPF4, NBPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258747
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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