A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587526



Internal ID16028249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474235..41475648hg38UCSC Ensembl
Innerchr21:42846162..42847575hg19UCSC Ensembl
Innerchr21:41768032..41769445hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381414
hg191414
hg181414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7840n54
Supporting Variantsnssv947011, nssv947009, nssv947012, nssv947008, nssv947006, nssv947010, nssv947013, nssv947007
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587526
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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