A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021768



Internal ID21931111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19738684..19739499hg38UCSC Ensembl
chr17:19641997..19642812hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633008
Samples
Known GenesALDH3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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