A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156656



Internal ID22087057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39514211..39526962hg38UCSC Ensembl
Outerchr7:39510390..39530900hg38UCSC Ensembl
Innerchr7:39553810..39566561hg19UCSC Ensembl
Outerchr7:39549989..39570499hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3820511
hg1920511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021102
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156656
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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