A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013302



Internal ID19102520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77215098..77271165hg38UCSC Ensembl
Innerchr4:78136251..78192318hg19UCSC Ensembl
Innerchr4:78355275..78411342hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3856068
hg1956068
hg1856068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633839
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)nsv1013302
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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