A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735829



Internal ID20511772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91557163..91557342hg38UCSC Ensembl
chr14:92023507..92023686hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735829
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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