A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999596



Internal ID19159133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154522972..154598218hg38UCSC Ensembl
Innerchr3:154240761..154316007hg19UCSC Ensembl
Innerchr3:155723455..155798701hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3875247
hg1975247
hg1875247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741547
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)nsv999596
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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