A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350265



Internal ID22575934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203995740..203999090hg38UCSC Ensembl
chr1:203964868..203968218hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383351
hg193351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972981
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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