A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001367



Internal ID18743898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4124049..4237761hg38UCSC Ensembl
Innerchr3:4165733..4279445hg19UCSC Ensembl
Innerchr3:4140733..4254445hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38113713
hg19113713
hg18113713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4654n100
Supporting Variantsnssv3739576
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)nsv1001367
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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