A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450563



Internal ID22508434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68605915..68633122hg38UCSC Ensembl
chrX:67825757..67852964hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3827208
hg1927208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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