A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006027



Internal ID19095245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..102036hg38UCSC Ensembl
Innerchr3:60333..143719hg19UCSC Ensembl
Innerchr3:35333..118719hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3883382
hg1983387
hg1883387
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593534, nssv3593535, nssv3593536
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)nsv1006027
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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