A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009919



Internal ID19099138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64543610..64607051hg38UCSC Ensembl
Innerchr4:65409328..65472769hg19UCSC Ensembl
Innerchr4:65091923..65155364hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3863442
hg1963442
hg1863442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625950
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)nsv1009919
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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