A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045972



Internal ID21955224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3674468..3674540hg38UCSC Ensembl
chr19:3674466..3674538hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620323
Samples
Known GenesPIP5K1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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