A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257209



Internal ID21400493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72820119..72890618hg38UCSC Ensembl
chrX:72039953..72110442hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3870500
hg1970490
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)nssv16257209
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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