A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026264



Internal ID21935607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4469841..4471082hg38UCSC Ensembl
chr16:4519842..4521083hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602046
Samples
Known GenesNMRAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026264
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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