A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003145



Internal ID18745677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046103..4087317hg38UCSC Ensembl
Innerchr3:4087787..4129001hg19UCSC Ensembl
Innerchr3:4062787..4104001hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3841215
hg1941215
hg1841215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4643n100
Supporting Variantsnssv3590425, nssv3590424
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)nsv1003145
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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