A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009299



Internal ID18751830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197916770..198018555hg38UCSC Ensembl
Innerchr3:197643641..197745426hg19UCSC Ensembl
Innerchr3:199128038..199229823hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38101786
hg19101786
hg18101786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3617031
Samples
Known GenesIQCG, LMLN, RPL35A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009299
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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