A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004824



Internal ID19094041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77267538..77391820hg38UCSC Ensembl
Innerchr4:78188691..78312974hg19UCSC Ensembl
Innerchr4:78407715..78531998hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38124283
hg19124284
hg18124284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5326n100
Supporting Variantsnssv3633870
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)nsv1004824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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