A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256219



Internal ID21397847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149742548..149770939hg38UCSC Ensembl
chrX:148824209..148852600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828392
hg1928392
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256219
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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