A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256932



Internal ID21397931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152755383..152767294hg38UCSC Ensembl
chrX:151923907..151935810hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3811912
hg1911904
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730087
Supporting Variants
SamplesHG00512
Known GenesCSAG2, CSAG3, MAGEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256932
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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