A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970079



Internal ID22745014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95139718..95189136hg38UCSC Ensembl
chrX:94394717..94444135hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3849419
hg1949419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461417
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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