A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010490



Internal ID19099707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164243312..164681437hg38UCSC Ensembl
Innerchr3:163961100..164399225hg19UCSC Ensembl
Innerchr3:165443794..165881919hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38438126
hg19438126
hg18438126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614538
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)nsv1010490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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