A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368607



Internal ID22594276
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 StatusS
Merged Variantsnsv5969471
Supporting Variants
Samples
Known GenesXCL1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368607
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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