A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066749



Internal ID19155968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1591066..1613191hg38UCSC Ensembl
Innerchr20:1571712..1593837hg19UCSC Ensembl
Innerchr20:1519712..1541837hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3822126
hg1922126
hg1822126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4236n100
Supporting Variantsnssv3599315, nssv3734844, nssv3599325, nssv3734847, nssv3599319, nssv3734846, nssv3734845, nssv3599314, nssv3599322, nssv3599318, nssv3599316, nssv3599320, nssv3599317, nssv3734843, nssv3599323, nssv3599326, nssv3599321, nssv3599324
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066749
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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