A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398325



Internal ID22456195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9766605..9801132hg38UCSC Ensembl
chr19:9877281..9911808hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3834528
hg1934528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968006
Supporting Variants
Samples
Known GenesZNF846
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398325
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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