A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004164



Internal ID19093381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..49308hg38UCSC Ensembl
Innerchr4:12269..49203hg19UCSC Ensembl
Innerchr4:2269..39203hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3837040
hg1936935
hg1836935
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5053n100
Supporting Variantsnssv3619240, nssv3619245, nssv3619249, nssv3737922, nssv3619244, nssv3619247, nssv3619246, nssv3737921, nssv3619243, nssv3619248, nssv3619242, nssv3619241
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)nsv1004164
Frequency
Sample Size11257
Observed Gain9
Observed Loss3
Observed Complex0
Frequencyn/a


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