A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011059



Internal ID22072690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43592920..43646608hg38UCSC Ensembl
Outerchr15:43553305..43684220hg38UCSC Ensembl
Innerchr15:43885118..43938806hg19UCSC Ensembl
Outerchr15:43845503..43976418hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38130916
hg19130916
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155167
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011059
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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