A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156694



Internal ID22087095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86604868..86615738hg38UCSC Ensembl
Outerchr7:86600286..86622960hg38UCSC Ensembl
Innerchr7:86234184..86245054hg19UCSC Ensembl
Outerchr7:86229602..86252276hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3822675
hg1922675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022157, nssv4022160, nssv4022161, nssv4022158, nssv4022159, nssv4022162
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156694
Frequency
Sample Size131
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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