A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156007



Internal ID22086512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103226498..103232318hg38UCSC Ensembl
Outerchr3:103219973..103244137hg38UCSC Ensembl
Innerchr3:102945342..102951162hg19UCSC Ensembl
Outerchr3:102938817..102962981hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3824165
hg1924165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017810, nssv4017811
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156007
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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