A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747904



Internal ID21387948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28985647..28991341hg38UCSC Ensembl
chr11:29007194..29012888hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg385695
hg195695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431486
Supporting Variants
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747904
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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