A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035177



Internal ID21944520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60147971..60160010hg38UCSC Ensembl
chr14:60614689..60626728hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3812040
hg1912040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617215
Samples
Known GenesDHRS7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035177
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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