A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792844



Internal ID21238182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85879566..85879566hg38UCSC Ensembl
chr12:86273344..86273344hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683992
Samples
Known GenesNTS
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792844
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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