A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751488



Internal ID21387563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11903118..11903445hg38UCSC Ensembl
chr6:11903351..11903678hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434733
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751488
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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