A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015049



Internal ID19104266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:124115935..124471912hg38UCSC Ensembl
Innerchr4:125037090..125393067hg19UCSC Ensembl
Innerchr4:125256540..125612517hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38355978
hg19355978
hg18355978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639406
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)nsv1015049
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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