A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406005



Internal ID22463875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20770935..20970953hg38UCSC Ensembl
chr19:20953741..21153759hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38200019
hg19200019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970427
Supporting Variants
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406005
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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