A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058886



Internal ID18801417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37969257..38427716hg38UCSC Ensembl
Innerchr21:39341560..39799638hg19UCSC Ensembl
Innerchr21:38263430..38721508hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38458460
hg19458079
hg18458079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600193
Samples
Known GenesDSCR10, DSCR4, DSCR8, ERG, KCNJ15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058886
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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