A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010009



Internal ID18752540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:83548743..83961375hg38UCSC Ensembl
Innerchr4:84469896..84882528hg19UCSC Ensembl
Innerchr4:84688920..85101552hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38412633
hg19412633
hg18412633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742874
Samples
Known GenesAGPAT9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010009
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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