A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156657



Internal ID22087058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39827243..39924047hg38UCSC Ensembl
Outerchr7:39825474..39924289hg38UCSC Ensembl
Innerchr7:39866842..39963646hg19UCSC Ensembl
Outerchr7:39865073..39963888hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3898816
hg1998816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021103
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156657
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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