A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970424



Internal ID22745359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16081187..16082403hg38UCSC Ensembl
chr1:16407682..16408898hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350154
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970424
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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