A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011542



Internal ID19100759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..45550hg38UCSC Ensembl
Innerchr3:60333..87232hg19UCSC Ensembl
Innerchr3:35333..62232hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3826896
hg1926900
hg1826900
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4600n100
Supporting Variantsnssv3593479, nssv3593478, nssv3593480
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)nsv1011542
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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