A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256936



Internal ID21399512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153074419..153075613hg38UCSC Ensembl
chrX:152242802..152243996hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730132
Supporting Variants
SamplesHG00733
Known GenesPNMA6C
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256936
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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