A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946778



Internal ID16240734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39312501..39334668hg38UCSC Ensembl
Innerchr21:40684427..40706594hg19UCSC Ensembl
Innerchr21:39606297..39628464hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3822168
hg1922168
hg1822168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587482
Supporting Variants
Samples
Known GenesBRWD1, BRWD1-AS1, BRWD1-IT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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