A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364264



Internal ID22589933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96101121..96101217hg38UCSC Ensembl
chr12:96494899..96494995hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364264
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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