A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012781



Internal ID19101998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..81831hg38UCSC Ensembl
Innerchr3:60333..123514hg19UCSC Ensembl
Innerchr3:35333..98514hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3863177
hg1963182
hg1863182
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4603n100
Supporting Variantsnssv3593524, nssv3593525
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)nsv1012781
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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