A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640897



Internal ID21832944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141585257..141589189hg38UCSC Ensembl
chrX:140673379..140677316hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg383933
hg193938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102339
Supporting Variants
Samples
Known GenesSPANXA2-OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640897
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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