A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012178



Internal ID22073809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85968474..85977902hg38UCSC Ensembl
Outerchr15:85965728..85978606hg38UCSC Ensembl
Innerchr15:86511705..86521133hg19UCSC Ensembl
Outerchr15:86508959..86521837hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3812879
hg1912879
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155203
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012178
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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