A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065126



Internal ID18807657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45466796..45556768hg38UCSC Ensembl
Innerchr21:46886710..46976682hg19UCSC Ensembl
Innerchr21:45711138..45801110hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3889973
hg1989973
hg1889973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4438n100
Supporting Variantsnssv3600247, nssv3600249, nssv3600248, nssv3600252, nssv3600251, nssv3600259, nssv3600257, nssv3600255, nssv3600244, nssv3600250, nssv3600245, nssv3600254, nssv3600243, nssv3600253, nssv3600241, nssv3600258, nssv3600242, nssv3600246, nssv3600256
Samples
Known GenesCOL18A1, MIR6815, SLC19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065126
Frequency
Sample Size29084
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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