A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009018



Internal ID19098236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144078841..144149508hg38UCSC Ensembl
Innerchr3:143797683..143868350hg19UCSC Ensembl
Innerchr3:145280373..145351040hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3870668
hg1970668
hg1870668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4914n100
Supporting Variantsnssv3606131
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)nsv1009018
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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