A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258155



Internal ID21400524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51669469..51713883hg38UCSC Ensembl
chrX:51412401..51456979hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3844415
hg1944579
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730130
Supporting Variants
SamplesNA19240
Known GenesCENPVP1, CENPVP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258155
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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