A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998405



Internal ID19157941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99210576..99233599hg38UCSC Ensembl
Innerchr3:98929420..98952443hg19UCSC Ensembl
Innerchr3:100412110..100435133hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3823024
hg1923024
hg1823024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4823n100
Supporting Variantsnssv3603460
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)nsv998405
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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