A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366218



Internal ID22591887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65716416..65719028hg38UCSC Ensembl
chr12:66110196..66112808hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg382613
hg192613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366218
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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