A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004588



Internal ID22066219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11901648..11993394hg38UCSC Ensembl
Outerchr10:11897482..11996036hg38UCSC Ensembl
Innerchr10:11943647..12035393hg19UCSC Ensembl
Outerchr10:11939481..12038035hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3898555
hg1998555
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154551
Supporting Variants
Samples
Known GenesUPF2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004588
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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