A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512268



Internal ID20885600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84647301..84650000hg38UCSC Ensembl
chr16:84680907..84683606hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190233
Samples
Known GenesKLHL36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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