A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036612



Internal ID21945955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95545680..95547800hg38UCSC Ensembl
chr14:96012017..96014137hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382121
hg192121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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