A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696025



Internal ID21217877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125706479..125706479hg38UCSC Ensembl
chr12:126191025..126191025hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696025
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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