A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979328



Internal ID22754263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32019307..33218671hg38UCSC Ensembl
chr19:32510213..33709577hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381199365
hg191199365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391275
Samples
Known GenesANKRD27, C19orf40, CEP89, DPY19L3, GPATCH1, LOC400684, LRP3, NUDT19, PDCD5, RGS9BP, RHPN2, SLC7A10, SLC7A9, TDRD12, WDR88, ZNF507
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979328
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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