A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970157



Internal ID22745092
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 StatusM
Merged Variants
Supporting Variantsnssv17452963
Samples
Known GenesLOC92249
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970157
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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