A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156641



Internal ID22087042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9939699..10019467hg38UCSC Ensembl
Outerchr7:9929443..10024876hg38UCSC Ensembl
Innerchr7:9979326..10059094hg19UCSC Ensembl
Outerchr7:9969073..10064503hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3895434
hg1995431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021049
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156641
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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