A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023782



Internal ID21933125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39001521..39001605hg38UCSC Ensembl
chr14:39470725..39470809hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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