A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3612701



Internal ID18910982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:170668981..170878001hg38UCSC Ensembl
Innerchr3:170386770..170595790hg19UCSC Ensembl
Innerchr3:171869464..172078484hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38209021
hg19209021
hg18209021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012255
Supporting Variants
Samples
Known GenesRPL22L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3612701
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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