A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973723



Internal ID22748658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140282460..140283743hg38UCSC Ensembl
chr7:139982260..139983543hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381284
hg191284
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445064
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973723
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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