A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545918



Internal ID16333327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28244295..28281105hg38UCSC Ensembl
Innerchr1:28570806..28607616hg19UCSC Ensembl
Innerchr1:28443393..28480203hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3836811
hg1936811
hg1836811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712051
Samples
Known GenesSESN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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