A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260330



Internal ID20469548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73647604..73647604hg38UCSC Ensembl
chr6:74357327..74357327hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766596
Supporting Variants
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260330
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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