A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271332



Internal ID20480550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52408970..52408970hg38UCSC Ensembl
chr12:52802754..52802754hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271332
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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