A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006253



Internal ID19095471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26491082..26560273hg38UCSC Ensembl
Innerchr3:26532573..26601764hg19UCSC Ensembl
Innerchr3:26507577..26576768hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3869192
hg1969192
hg1869192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4710n100
Supporting Variantsnssv3589549, nssv3589548, nssv3589546, nssv3589547
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006253
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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