A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792484



Internal ID21237822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6403565..6403565hg38UCSC Ensembl
chr12:6512731..6512731hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681382, nssv13692975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792484
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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