A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978526



Internal ID22753461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53514955..53544238hg38UCSC Ensembl
chr7:53582648..53611931hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3829284
hg1929284
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440981
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978526
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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