A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008193



Internal ID18750724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62720166..63275670hg38UCSC Ensembl
Innerchr4:63585884..64141388hg19UCSC Ensembl
Innerchr4:63268479..63823983hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38555505
hg19555505
hg18555505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5222n100
Supporting Variantsnssv3626525
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)nsv1008193
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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