A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3617031



Internal ID18568626
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 StatusS
Merged Variantsnsv1009299
Supporting Variants
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)nssv3617031
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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