A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009794



Internal ID22071425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24201200..24289879hg38UCSC Ensembl
Outerchr15:24197072..24297086hg38UCSC Ensembl
Innerchr15:24446347..24535026hg19UCSC Ensembl
Outerchr15:24442219..24542233hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38100015
hg19100015
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155105
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009794
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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