A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065873



Internal ID18808404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10469623..10611996hg38UCSC Ensembl
Innerchr21:10900461..11042834hg19UCSC Ensembl
Innerchr21:9922332..10064705hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38142374
hg19142374
hg18142374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4356n100
Supporting Variantsnssv3732532
Samples
Known GenesBAGE2, 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)nsv1065873
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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