A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008920



Internal ID19098138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162320062..162405566hg38UCSC Ensembl
Innerchr3:162037850..162123354hg19UCSC Ensembl
Innerchr3:163520544..163606048hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3885505
hg1985505
hg1885505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607946
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)nsv1008920
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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