A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977458



Internal ID22752393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145968495..145973446hg38UCSC Ensembl
chr7:145665588..145670539hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384952
hg194952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445624
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977458
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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