A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038643



Internal ID21947986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82580312..82580384hg38UCSC Ensembl
chr17:80538188..80538260hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635649
Samples
Known GenesFOXK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038643
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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