A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063957



Internal ID19153176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45670561..45748377hg38UCSC Ensembl
Innerchr21:47090475..47168291hg19UCSC Ensembl
Innerchr21:45914903..45992719hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3877817
hg1977817
hg1877817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3733461
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)nsv1063957
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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