A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005250



Internal ID21914593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169553024..169553100hg38UCSC Ensembl
chr6:169953120..169953196hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576038
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005250
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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