A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258573



Internal ID21399874
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730276
Supporting Variants
SamplesNA19238
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258573
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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