A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997266



Internal ID19156804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121404899..121491079hg38UCSC Ensembl
Innerchr4:122326054..122412234hg19UCSC Ensembl
Innerchr4:122545504..122631684hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3886181
hg1986181
hg1886181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5379n100
Supporting Variantsnssv3639380
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)nsv997266
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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