A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258490



Internal ID21400410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72855897..72874910hg38UCSC Ensembl
chrX:72075760..72094744hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3819014
hg1918985
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730263
Supporting Variants
SamplesNA19239
Known GenesDMRTC1, DMRTC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258490
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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