A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156718



Internal ID22087119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116356802..116392692hg38UCSC Ensembl
Outerchr7:116349587..116400485hg38UCSC Ensembl
Innerchr7:115996856..116032746hg19UCSC Ensembl
Outerchr7:115989641..116040539hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3850899
hg1950899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022224
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156718
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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