A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998464



Internal ID18811314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4079539..4118028hg38UCSC Ensembl
Innerchr3:4121223..4159712hg19UCSC Ensembl
Innerchr3:4096223..4134712hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3838490
hg1938490
hg1838490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4649n100
Supporting Variantsnssv3590451, nssv3590449, nssv3590452, nssv3590448, nssv3590454, nssv3590450, nssv3590447, nssv3590453
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)nsv998464
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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