A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454955



Internal ID22269864
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3551146
Supporting Variants
SamplesNA19239
Known GenesDMRTC1, DMRTC1B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454955
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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