A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001049



Internal ID19090266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48808840..49352968hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg18544129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5205n100
Supporting Variantsnssv3739419, nssv3625206
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)nsv1001049
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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