A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018209



Internal ID18760742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166576123..166741989hg38UCSC Ensembl
Innerchr4:167497275..167663140hg19UCSC Ensembl
Innerchr4:167716725..167899715hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38165867
hg19165866
hg18182991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634175
Samples
Known GenesSPOCK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018209
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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