A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009700



Internal ID19098918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17349748..17445179hg38UCSC Ensembl
Innerchr3:17391240..17486671hg19UCSC Ensembl
Innerchr3:17366244..17461675hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3895432
hg1995432
hg1895432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739637
Samples
Known GenesTBC1D5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009700
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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