A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156736



Internal ID22087137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143520153..143728285hg38UCSC Ensembl
Innerchr7:143218408..143408430hg19UCSC Ensembl
Outerchr7:143217246..143425378hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38208133
hg19208133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv270n97
Supporting Variantsnssv4022456
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156736
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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