A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156646



Internal ID22087047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13547787..13552049hg38UCSC Ensembl
Outerchr7:13543641..13558316hg38UCSC Ensembl
Innerchr7:13587412..13591674hg19UCSC Ensembl
Outerchr7:13583266..13597941hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3814676
hg1914676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021055
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156646
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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