A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603576



Internal ID21795623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25370437..25370437hg38UCSC Ensembl
chr12:25523371..25523371hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094519
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603576
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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