A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015820



Internal ID21925163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148261362..148308517hg38UCSC Ensembl
chr5:147640925..147688080hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3847156
hg1947156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560675
Samples
Known GenesLOC102546294, SPINK13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015820
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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