A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156060



Internal ID22086565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188190920..188261228hg38UCSC Ensembl
Outerchr3:188185774..188261945hg38UCSC Ensembl
Innerchr3:187908708..187979016hg19UCSC Ensembl
Outerchr3:187903562..187979733hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3876172
hg1976172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017224
Samples
Known GenesLPP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156060
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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