A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998039



Internal ID19157576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77249164..77336869hg38UCSC Ensembl
Innerchr4:78170317..78258022hg19UCSC Ensembl
Innerchr4:78389341..78477046hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3887706
hg1987706
hg1887706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5323n100
Supporting Variantsnssv3633858
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)nsv998039
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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