A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154604



Internal ID22085109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17454768..17520426hg38UCSC Ensembl
Outerchr1:17450337..17523436hg38UCSC Ensembl
Innerchr1:17781264..17846922hg19UCSC Ensembl
Outerchr1:17776833..17849932hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3873100
hg1973100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007063
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154604
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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