A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042731



Internal ID21952043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44696995..44697112hg38UCSC Ensembl
chr21:46116910..46117027hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643272
Samples
Known GenesTSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042731
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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