A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036124



Internal ID21945467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30105850..30105908hg38UCSC Ensembl
chr16:30117171..30117229hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635164
Samples
Known GenesGDPD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036124
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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