A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156740



Internal ID22087141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525988..143835905hg38UCSC Ensembl
Outerchr7:143521875..143846758hg38UCSC Ensembl
Innerchr7:143223081..143532998hg19UCSC Ensembl
Outerchr7:143218968..143543851hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38324884
hg19324884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019591, nssv4019590
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C, LOC154761
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156740
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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