A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000299



Internal ID19089516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113433086..113444560hg38UCSC Ensembl
Innerchr4:114354242..114365716hg19UCSC Ensembl
Innerchr4:114573691..114585165hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3811475
hg1911475
hg1811475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5359n100
Supporting Variantsnssv3632708
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)nsv1000299
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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