A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025169



Internal ID21934512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77220005..77220075hg38UCSC Ensembl
chr11:76931050..76931120hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579291
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025169
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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