A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034290



Internal ID21943633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21258463..21261886hg38UCSC Ensembl
chr16:21269784..21273207hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg383424
hg193424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607124
Samples
Known GenesCRYM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034290
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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