A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028146



Internal ID18770677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185582745..186417181hg38UCSC Ensembl
Innerchr4:186503899..187338335hg19UCSC Ensembl
Innerchr4:186740893..187575329hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38834437
hg19834437
hg18834437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635625
Samples
Known GenesCYP4V2, F11, F11-AS1, FAM149A, FLJ38576, KLKB1, SORBS2, TLR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028146
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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