A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062862



Internal ID18805393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14248070..14276911hg38UCSC Ensembl
Innerchr21:15620391..15649232hg19UCSC Ensembl
Innerchr21:14542262..14571103hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3828842
hg1928842
hg1828842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4389n100
Supporting Variantsnssv3586458
Samples
Known GenesABCC13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062862
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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