A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974294



Internal ID22749229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150085664..150086109hg38UCSC Ensembl
chrX:149253895..149254340hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443460
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974294
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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