A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419083



Internal ID22476953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73754603..73769737hg38UCSC Ensembl
chr4:74620320..74635454hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3815135
hg1915135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419083
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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