A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156340



Internal ID22084816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108937665..108955523hg38UCSC Ensembl
Outerchr1:108930299..108961034hg38UCSC Ensembl
Innerchr1:109480287..109498145hg19UCSC Ensembl
Outerchr1:109472921..109503656hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3830736
hg1930736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021404
Samples
Known GenesCLCC1, GPSM2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156340
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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