A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007235



Internal ID19096454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195855597..195925040hg38UCSC Ensembl
Innerchr3:195582468..195651911hg19UCSC Ensembl
Innerchr3:197066865..197136308hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3869444
hg1969444
hg1869444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616985
Samples
Known GenesMIR6829, TNK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007235
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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