A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063484



Internal ID18806015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10420787..10545487hg38UCSC Ensembl
Innerchr21:10966970..11091670hg19UCSC Ensembl
Innerchr21:9988841..10113541hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38124701
hg19124701
hg18124701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4367n100
Supporting Variantsnssv3585090
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063484
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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