A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155167



Internal ID22085672
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011059, nssv4011058
Samples
Known GenesCATSPER2, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155167
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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