A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010233



Internal ID18752764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4099559..4162139hg38UCSC Ensembl
Innerchr3:4141243..4203823hg19UCSC Ensembl
Innerchr3:4116243..4178823hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3862581
hg1962581
hg1862581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4651n100
Supporting Variantsnssv3590461
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)nsv1010233
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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