A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003496



Internal ID21912839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178594947..178622046hg38UCSC Ensembl
chr5:178021948..178049047hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3827100
hg1927100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562760
Samples
Known GenesCLK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003496
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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