A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003169



Internal ID21912512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165334382..165334479hg38UCSC Ensembl
chr6:165747871..165747968hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557622
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003169
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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