A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033768



Internal ID21943111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50259171..50259226hg38UCSC Ensembl
chr17:48336532..48336587hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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