A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156497



Internal ID22086898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40098471..40133607hg38UCSC Ensembl
Outerchr6:40095143..40134852hg38UCSC Ensembl
Innerchr6:40066210..40101346hg19UCSC Ensembl
Outerchr6:40062882..40102591hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3839710
hg1939710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv248n97
Supporting Variantsnssv4018554
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156497
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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