A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006867



Internal ID19096085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9455251..9711988hg38UCSC Ensembl
Innerchr4:9456977..9713612hg19UCSC Ensembl
Innerchr4:9066075..9322710hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38256738
hg19256636
hg18256636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5104n100
Supporting Variantsnssv3738205
Samples
Known GenesLOC650293, MIR548I2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006867
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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