A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017552



Internal ID21926895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132905943..132908769hg38UCSC Ensembl
chr5:132241635..132244461hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382827
hg192827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547208
Samples
Known GenesAFF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017552
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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