A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008873



Internal ID18751404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142102091..142275700hg38UCSC Ensembl
Innerchr3:141820933..141994542hg19UCSC Ensembl
Innerchr3:143303623..143477232hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38173610
hg19173610
hg18173610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606105
Samples
Known GenesGK5, TFDP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008873
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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