A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008866



Internal ID19098084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136645669..136708948hg38UCSC Ensembl
Innerchr3:136364511..136427790hg19UCSC Ensembl
Innerchr3:137847201..137910480hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3863280
hg1963280
hg1863280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607148
Samples
Known GenesSTAG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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