A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015023



Internal ID18757558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103117988..103644060hg38UCSC Ensembl
Innerchr4:104039145..104565217hg19UCSC Ensembl
Innerchr4:104258594..104784666hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38526073
hg19526073
hg18526073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631032
Samples
Known GenesCENPE, TACR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015023
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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