A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997890



Internal ID19157426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5052136..5089711hg38UCSC Ensembl
Innerchr3:5093821..5131396hg19UCSC Ensembl
Innerchr3:5068821..5106396hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3837576
hg1937576
hg1837576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591637
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)nsv997890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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