A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004448



Internal ID21913791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165463056..165477777hg38UCSC Ensembl
chr6:165876544..165891265hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3814722
hg1914722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572327
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004448
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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