A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002097



Internal ID21911440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59381238..59410187hg38UCSC Ensembl
chr5:58677064..58706013hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3828950
hg1928950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538343
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002097
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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