A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027921



Internal ID18770452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188472958..189614444hg38UCSC Ensembl
Innerchr4:189394112..190535598hg19UCSC Ensembl
Innerchr4:189631106..190772592hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381141487
hg191141487
hg181141487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744548
Samples
Known GenesLINC01060
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027921
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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