A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038657



Internal ID21948000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96886629..96897431hg38UCSC Ensembl
chr14:97352966..97363768hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810803
hg1910803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038657
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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