A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156719



Internal ID22087120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116673783..116810801hg38UCSC Ensembl
Outerchr7:116665807..116812838hg38UCSC Ensembl
Innerchr7:116313837..116450855hg19UCSC Ensembl
Outerchr7:116305861..116452892hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38147032
hg19147032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022225
Samples
Known GenesMET
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156719
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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