A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999594



Internal ID18812444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17648924..17940826hg38UCSC Ensembl
Innerchr3:17690416..17982318hg19UCSC Ensembl
Innerchr3:17665420..17957322hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38291903
hg19291903
hg18291903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593096
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)nsv999594
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer