A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600299



Internal ID18898580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45894976..45923450hg38UCSC Ensembl
Innerchr21:47314890..47343364hg19UCSC Ensembl
Innerchr21:46139318..46167792hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3828475
hg1928475
hg1828475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062386
Supporting Variants
Samples
Known GenesPCBP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600299
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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