A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035660



Internal ID21945003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29893396..29893490hg38UCSC Ensembl
chr16:29904717..29904811hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626619
Samples
Known GenesSEZ6L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035660
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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