A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003618



Internal ID18746149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102609308..102641004hg38UCSC Ensembl
Innerchr4:103530465..103562161hg19UCSC Ensembl
Innerchr4:103749503..103781209hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3831697
hg1931697
hg1831707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631030, nssv3631029
Samples
Known GenesMANBA, NFKB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003618
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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