A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035618



Internal ID21944961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102340042..102340341hg38UCSC Ensembl
chr14:102806379..102806678hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613077
Samples
Known GenesZNF839
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035618
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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