A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452963



Internal ID22510836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63462007..63465854hg38UCSC Ensembl
chrX:62681887..62685734hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg383848
hg193848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970157
Supporting Variants
Samples
Known GenesLOC92249
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452963
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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