A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391275



Internal ID22449145
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 StatusS
Merged Variantsnsv5979328
Supporting Variants
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)nssv17391275
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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