A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011068



Internal ID22072699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46838203..46924708hg38UCSC Ensembl
Outerchr15:46836155..46929167hg38UCSC Ensembl
Innerchr15:47130401..47216906hg19UCSC Ensembl
Outerchr15:47128353..47221365hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3893013
hg1993013
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011068
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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