A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257378



Internal ID21399890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101599387..101611782hg38UCSC Ensembl
chrX:100854365..100866772hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3812396
hg1912408
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730113
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257378
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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