A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155189



Internal ID22085694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72617073..72631368hg38UCSC Ensembl
Outerchr15:72610997..72670944hg38UCSC Ensembl
Innerchr15:72909414..72923709hg19UCSC Ensembl
Outerchr15:72903338..72963285hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3859948
hg1959948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011106
Samples
Known GenesGOLGA6B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155189
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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