A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008694



Internal ID19097911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:23650835..23718839hg38UCSC Ensembl
Innerchr4:23652458..23720462hg19UCSC Ensembl
Innerchr4:23261556..23329560hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3868005
hg1968005
hg1868005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5156n100
Supporting Variantsnssv3620589
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)nsv1008694
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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