A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011644



Internal ID18754178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760743..46808087hg38UCSC Ensembl
Innerchr3:46802233..46849577hg19UCSC Ensembl
Innerchr3:46777237..46824581hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3847345
hg1947345
hg1847345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3593796, nssv3593798, nssv3593794, nssv3593797, nssv3593795
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)nsv1011644
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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