A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936964



Internal ID22712325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:58664173..58674542hg38UCSC Ensembl
chr12:59057955..59068324hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3810370
hg1910370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936964
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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