A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585250



Internal ID16372659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1588894..1611843hg38UCSC Ensembl
Innerchr20:1569540..1592489hg19UCSC Ensembl
Innerchr20:1517540..1540489hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3822950
hg1922950
hg1822950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7434n54
Supporting Variantsnssv936668, nssv936646, nssv936673, nssv936665, nssv936653, nssv936657, nssv936651, nssv936641, nssv936647, nssv936663, nssv936640, nssv936664, nssv936670, nssv936649, nssv936662, nssv936667, nssv936661, nssv936643, nssv936656, nssv936672, nssv936655, nssv936645, nssv936669, nssv936648, nssv936671, nssv936652, nssv936650, nssv936644, nssv936666, nssv936658, nssv936660, nssv936659, nssv936654, nssv936642
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585250
Frequency
Sample Size17421
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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