A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998636



Internal ID21907979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84650241..84650409hg38UCSC Ensembl
chr4:85571394..85571562hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538143
Samples
Known GenesCDS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998636
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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