A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044486



Internal ID21953768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21249564..22771714hg38UCSC Ensembl
chr19:21432366..22954516hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381522151
hg191522151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv26n212
Supporting Variantsnssv17636770
Samples
Known GenesLINC00664, LOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF492, ZNF493, ZNF676, ZNF708, ZNF729, ZNF738, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044486
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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