A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156575



Internal ID22086976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112595825..112608342hg38UCSC Ensembl
Outerchr6:112591729..112610754hg38UCSC Ensembl
Innerchr6:112917027..112929544hg19UCSC Ensembl
Outerchr6:112912931..112931956hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3819026
hg1919026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022625
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156575
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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