A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977817



Internal ID22752752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23587020..23678598hg38UCSC Ensembl
chr7:23626639..23718217hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3891579
hg1991579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436996
Samples
Known GenesCCDC126
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977817
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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