A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265647



Internal ID20474865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6403569..6403569hg38UCSC Ensembl
chr12:6512735..6512735hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265647
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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