A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011010



Internal ID19100227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152624726..152638401hg38UCSC Ensembl
Innerchr3:152342515..152356190hg19UCSC Ensembl
Innerchr3:153825205..153838880hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3813676
hg1913676
hg1813676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4923n100
Supporting Variantsnssv3606338, nssv3606339, nssv3606340
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)nsv1011010
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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