A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257125



Internal ID21399256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52499085..52538369hg38UCSC Ensembl
chrX:52242227..52567379hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3839285
hg19325153
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730276
Supporting Variants
SamplesHG00732
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257125
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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