A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560675



Internal ID21885030
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 StatusS
Merged Variantsnsv6015820
Supporting Variants
Samples
Known GenesLOC102546294, SPINK13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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