A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000055



Internal ID19089272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182644010..182661738hg38UCSC Ensembl
Innerchr3:182361798..182379526hg19UCSC Ensembl
Innerchr3:183844492..183862220hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3817729
hg1917729
hg1817729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615001, nssv3615000
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)nsv1000055
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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