A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970369



Internal ID22745304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153317975..153575849hg38UCSC Ensembl
chrX:152583433..152841307hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38257875
hg19257875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434799
Samples
Known GenesATP2B3, BGN, HAUS7, TREX2, ZFP92, ZNF275
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970369
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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