A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968081



Internal ID22743016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144899066..144956312hg38UCSC Ensembl
chrX:143980586..144037832hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3857247
hg1957247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449220
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968081
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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