A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010365



Internal ID19099582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88855260..88901261hg38UCSC Ensembl
Innerchr3:88904410..88950411hg19UCSC Ensembl
Innerchr3:88987100..89033101hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3846002
hg1946002
hg1846002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596281
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)nsv1010365
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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