A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156653



Internal ID22087054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31525103..31594386hg38UCSC Ensembl
Outerchr7:31524565..31603340hg38UCSC Ensembl
Innerchr7:31564717..31634000hg19UCSC Ensembl
Outerchr7:31564179..31642954hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3878776
hg1978776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021099
Samples
Known GenesCCDC129
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156653
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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