A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258152



Internal ID21398145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52038080..52213115hg38UCSC Ensembl
chrX:51781176..51956242hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38175036
hg19175067
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730085
Supporting Variants
SamplesHG00513
Known GenesMAGED4, MAGED4B, SNORA11D, SNORA11E
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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