A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258465



Internal ID21399976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135147364..135236976hg38UCSC Ensembl
chrX:134281291..134370923hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3889613
hg1989633
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730233
Supporting Variants
SamplesNA19238
Known GenesCXorf48
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258465
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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