A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587515



Internal ID16028238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474022..41475648hg38UCSC Ensembl
Innerchr21:42845949..42847575hg19UCSC Ensembl
Innerchr21:41767819..41769445hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381627
hg191627
hg181627
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7839n54
Supporting Variantsnssv946954, nssv946948, nssv946958, nssv946959, nssv946945, nssv946953, nssv946950, nssv946947, nssv946946, nssv946960, nssv946949, nssv946955, nssv946957, nssv946952, nssv946944, nssv946951, nssv946956, nssv946943
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587515
Frequency
Sample Size17421
Observed Gain13
Observed Loss5
Observed Complex0
Frequencyn/a


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