A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004684



Internal ID21914027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147861594..147897807hg38UCSC Ensembl
chr5:147241157..147277370hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3836214
hg1936214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561355
Samples
Known GenesC5orf46, SCGB3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004684
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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