A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040250



Internal ID21949593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16382324..16382554hg38UCSC Ensembl
chr17:16285638..16285868hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624450
Samples
Known GenesUBB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040250
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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