A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064704



Internal ID19153923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580129..1609876hg38UCSC Ensembl
Innerchr20:1560775..1590522hg19UCSC Ensembl
Innerchr20:1508775..1538522hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829748
hg1929748
hg1829748
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3591598, nssv3592710, nssv3591600, nssv3591596, nssv3728421, nssv3592713, nssv3728422, nssv3592729, nssv3592728, nssv3592711, nssv3591599, nssv3592717, nssv3592730, nssv3592722, nssv3592721, nssv3592714, nssv3592715, nssv3592725, nssv3592709, nssv3592716, nssv3592724, nssv3592712, nssv3592727, nssv3591597, nssv3591601, nssv3592723, nssv3592726, nssv3592720, nssv3592718, nssv3592719
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)nsv1064704
Frequency
Sample Size11257
Observed Gain22
Observed Loss8
Observed Complex0
Frequencyn/a


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