A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010286



Internal ID19099503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194903088..194927508hg38UCSC Ensembl
Innerchr3:194623817..194648237hg19UCSC Ensembl
Innerchr3:196105106..196129526hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3824421
hg1924421
hg1824421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611378
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)nsv1010286
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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