A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032803



Internal ID21942146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4254675..4254740hg38UCSC Ensembl
chr16:4304676..4304741hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032803
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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