A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014633



Internal ID19103851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52988921..53000512hg38UCSC Ensembl
Innerchr3:53022937..53034528hg19UCSC Ensembl
Innerchr3:52997977..53009568hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3811592
hg1911592
hg1811592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4741n100
Supporting Variantsnssv3739878
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)nsv1014633
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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