A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066728



Internal ID18809259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43669996..43711842hg38UCSC Ensembl
Innerchr21:45089877..45131723hg19UCSC Ensembl
Innerchr21:43914305..43956151hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3841847
hg1941847
hg1841847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600218
Samples
Known GenesRRP1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066728
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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