A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792918



Internal ID21238256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94950282..94950591hg38UCSC Ensembl
chr12:95344058..95344367hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792918
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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