A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002816



Internal ID18745348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114411140..114611220hg38UCSC Ensembl
Innerchr4:115332296..115532376hg19UCSC Ensembl
Innerchr4:115551745..115751825hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38200081
hg19200081
hg18200081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639234
Samples
Known GenesUGT8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002816
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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