A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066443



Internal ID19155662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18685360..18706170hg38UCSC Ensembl
Innerchr21:20057678..20078488hg19UCSC Ensembl
Innerchr21:18979549..19000359hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3820811
hg1920811
hg1820811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599731, nssv3732624, nssv3599743, nssv3599734, nssv3599740, nssv3599735, nssv3599737, nssv3732616, nssv3732621, nssv3732622, nssv3599733, nssv3599744, nssv3732625, nssv3599738, nssv3599741, nssv3732626, nssv3599730, nssv3599739, nssv3732620, nssv3599736, nssv3732617, nssv3732615, nssv3599745, nssv3732627, nssv3599742, nssv3732618, nssv3732619, nssv3732623, nssv3599732
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066443
Frequency
Sample Size11257
Observed Gain29
Observed Loss0
Observed Complex0
Frequencyn/a


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