A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048671



Internal ID21957905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9731384..9731457hg38UCSC Ensembl
chr19:9842060..9842133hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048671
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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