A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394010



Internal ID22451880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33158747..33171455hg38UCSC Ensembl
chr19:33649653..33662361hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812709
hg1912709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979807
Supporting Variants
Samples
Known GenesWDR88
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394010
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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