A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373573



Internal ID22599242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73368321..73368506hg38UCSC Ensembl
chr14:73835029..73835214hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978831
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373573
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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