A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585328



Internal ID18536923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13334446..14256347hg38UCSC Ensembl
Innerchr21:14706767..15628668hg19UCSC Ensembl
Innerchr21:13628638..14550539hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38921902
hg19921902
hg18921902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058202
Supporting Variants
Samples
Known GenesANKRD20A11P, C21orf15, LIPI, LOC100288966, MIR3156-3, MIR8069, POTED, RBM11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585328
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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