A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013963



Internal ID19103182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102685515..102723925hg38UCSC Ensembl
Innerchr4:103606672..103645082hg19UCSC Ensembl
Innerchr4:103825720..103864128hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3838411
hg1938411
hg1838409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631031
Samples
Known GenesMANBA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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