A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999414



Internal ID19158951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110384279..110621333hg38UCSC Ensembl
Innerchr3:110103126..110340180hg19UCSC Ensembl
Innerchr3:111585816..111822870hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38237055
hg19237055
hg18237055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604410
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)nsv999414
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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