A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011551



Internal ID19100768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77199719..77283071hg38UCSC Ensembl
Innerchr4:78120872..78204224hg19UCSC Ensembl
Innerchr4:78339896..78423248hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3883353
hg1983353
hg1883353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5321n100
Supporting Variantsnssv3633831
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)nsv1011551
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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