A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6n97



Internal ID22815403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16505368..16685015hg38UCSC Ensembl
chr1:16831863..17011510hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38179648
hg19179648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156254, nsv1156268
Samples
Known GenesCROCCP2, LOC729574, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv6n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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