A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156254



Internal ID22084730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16518437..16643961hg38UCSC Ensembl
Outerchr1:16505368..16660356hg38UCSC Ensembl
Innerchr1:16844932..16970456hg19UCSC Ensembl
Outerchr1:16831863..16986851hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38154989
hg19154989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n97
Supporting Variantsnssv4019160
Samples
Known GenesCROCCP2, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156254
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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