A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431861



Internal ID21393863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95346832..95347848hg38UCSC Ensembl
chr12:95740608..95741624hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749749
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431861
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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