A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933444



Internal ID21353513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82580432..82580642hg38UCSC Ensembl
chr17:80538308..80538518hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175750
SamplesHG002
Known GenesFOXK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933444
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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