A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971068



Internal ID22746003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44576341..44578968hg38UCSC Ensembl
chrX:44435587..44438214hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg382628
hg192628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469222
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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