A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436026



Internal ID22493896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145450328..145472370hg38UCSC Ensembl
chr7:145147421..145169463hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3822043
hg1922043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436026
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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