A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740067



Internal ID20516042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42194804..42194951hg38UCSC Ensembl
chr17:40346822..40346969hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740067
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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