A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747072



Internal ID21385410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11306328..11326476hg38UCSC Ensembl
chr1:11366385..11386533hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3820149
hg1920149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432926
Supporting Variants
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747072
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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