A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042543



Internal ID21951859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14376413..14378452hg38UCSC Ensembl
chr21:15748734..15750773hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg382040
hg192040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638773
Samples
Known GenesHSPA13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042543
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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