A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016086



Internal ID21925429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100065176..100379309hg38UCSC Ensembl
chr5:99400880..99715013hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38314134
hg19314134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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