A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979948



Internal ID22754883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6732229..6739914hg38UCSC Ensembl
chrX:6650270..6657955hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg387686
hg197686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451785
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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