A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969471



Internal ID22744406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168576778..168609808hg38UCSC Ensembl
chr1:168546016..168579046hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3833031
hg1933031
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368607
Samples
Known GenesXCL1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969471
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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