A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970937



Internal ID22745872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14943786..14948408hg38UCSC Ensembl
chr1:15270282..15274904hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384623
hg194623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361190
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970937
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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