A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018387



Internal ID18760920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157038779..157843038hg38UCSC Ensembl
Innerchr4:157959931..158764190hg19UCSC Ensembl
Innerchr4:158179381..158983640hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38804260
hg19804260
hg18804260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744273
Samples
Known GenesGLRB, GRIA2, LOC340017
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018387
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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