A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231746



Internal ID22372321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52489201..52533696hg38UCSC Ensembl
chrX:52232344..52562706hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3844496
hg19330363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456768, nssv14466257, nssv14466225, nssv14466182, nssv14466796, nssv14464502, nssv14453580
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00513, HG00514
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231746
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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