A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431624



Internal ID21393626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104975279..104979901hg38UCSC Ensembl
chr12:105369057..105373679hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384623
hg194623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv182n172
Supporting Variantsnssv15750582
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431624
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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