A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047763



Internal ID21956996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21595490..23111764hg38UCSC Ensembl
chr19:21778292..23294566hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381516275
hg191516275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv26n212
Supporting Variantsnssv17617588
Samples
Known GenesLOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047763
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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