A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998811



Internal ID19158347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28807547..28833782hg38UCSC Ensembl
Innerchr3:28849038..28875273hg19UCSC Ensembl
Innerchr3:28824042..28850277hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3826236
hg1926236
hg1826236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589569
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)nsv998811
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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