A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972512



Internal ID22747447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164177000..164200978hg38UCSC Ensembl
chr5:163604006..163627984hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3823979
hg1923979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424220
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972512
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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