A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257364



Internal ID21399550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97437020..97460380hg38UCSC Ensembl
chr7:97066332..97089692hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3823361
hg1923361
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730264
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257364
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer