A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730263



Internal ID21401074
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258490, nssv16256444, nssv16257209
SamplesNA19239
Known GenesDMRTC1, DMRTC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730263
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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