A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002519



Internal ID18745051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4132155..4277895hg38UCSC Ensembl
Innerchr3:4173839..4319579hg19UCSC Ensembl
Innerchr3:4148839..4294579hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38145741
hg19145741
hg18145741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4652n100
Supporting Variantsnssv3591617
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)nsv1002519
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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