A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057754



Internal ID21966987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1464020..1464154hg38UCSC Ensembl
chr19:1464019..1464153hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622203
Samples
Known GenesAPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057754
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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