A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104496



Internal ID21291105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55811774..55818661hg38UCSC Ensembl
Innerchr1:56277447..56284334hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg386888
hg196888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117107
Supporting Variants
Samplessample7
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104496
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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