A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009599



Internal ID19098817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62975101..63280974hg38UCSC Ensembl
Innerchr4:63840819..64146692hg19UCSC Ensembl
Innerchr4:63523414..63829287hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38305874
hg19305874
hg18305874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5223n100
Supporting Variantsnssv3626529
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)nsv1009599
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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