A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010511



Internal ID19099728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52988839..53005461hg38UCSC Ensembl
Innerchr3:53022855..53039477hg19UCSC Ensembl
Innerchr3:52997895..53014517hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3816623
hg1916623
hg1816623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4740n100
Supporting Variantsnssv3739877, nssv3739876
Samples
Known GenesSFMBT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010511
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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