A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009573



Internal ID19098791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143177206..143240935hg38UCSC Ensembl
Innerchr3:142896048..142959777hg19UCSC Ensembl
Innerchr3:144378738..144442467hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3863730
hg1963730
hg1863730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741487
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)nsv1009573
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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