A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030766



Internal ID18773297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183305034..183948875hg38UCSC Ensembl
Innerchr4:184226187..184870028hg19UCSC Ensembl
Innerchr4:184463181..185107022hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38643842
hg19643842
hg18643842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635605
Samples
Known GenesCDKN2AIP, CLDN22, CLDN24, ING2, LOC389247, RWDD4, STOX2, TRAPPC11, WWC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030766
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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