A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595228



Internal ID16382637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114882261..114968082hg38UCSC Ensembl
Innerchr4:115803417..115889238hg19UCSC Ensembl
Innerchr4:116022866..116108687hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3885822
hg1985822
hg1885822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152828
SamplesHGDP00110
Known GenesNDST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595228
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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