A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023737



Internal ID21933080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1549239..1551649hg38UCSC Ensembl
chr16:1599240..1601650hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382411
hg192411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606380
Samples
Known GenesIFT140, TMEM204
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023737
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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