A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003582



Internal ID21912925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169638022..169638351hg38UCSC Ensembl
chr6:170038118..170038447hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566620
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003582
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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