A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001449



Internal ID19090666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52975363..53005088hg38UCSC Ensembl
Innerchr3:53009379..53039104hg19UCSC Ensembl
Innerchr3:52984419..53014144hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3829726
hg1929726
hg1829726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4739n100
Supporting Variantsnssv3595262
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)nsv1001449
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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