A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277295



Internal ID20486513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113015597..113015597hg38UCSC Ensembl
chr3:112734444..112734444hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750742
Supporting Variants
Samples
Known GenesC3orf17
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277295
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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