A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019989



Internal ID21929332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133009214..133009301hg38UCSC Ensembl
chr5:132344906..132344993hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548559
Samples
Known GenesZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019989
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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