A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040192



Internal ID21949535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12005868..12006161hg38UCSC Ensembl
chr16:12099725..12100018hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607077
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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