A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439372



Internal ID22497242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148743468..148744339hg38UCSC Ensembl
chr7:148440560..148441431hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974402
Supporting Variants
Samples
Known GenesCUL1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439372
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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