A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007021



Internal ID19096239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..46452hg38UCSC Ensembl
Innerchr4:12269..46448hg19UCSC Ensembl
Innerchr4:2269..36448hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834184
hg1934180
hg1834180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5051n100
Supporting Variantsnssv3619226
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007021
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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