A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604200



Internal ID21796247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57851949..57851949hg38UCSC Ensembl
chr12:58245732..58245732hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604200
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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