A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456034



Internal ID22513911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91134640..91146347hg38UCSC Ensembl
chr12:91528417..91540124hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3811708
hg1911708
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865080
Supporting Variants
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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