A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615657



Internal ID21807704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16510964..16510964hg38UCSC Ensembl
chr12:16663898..16663898hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615657
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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