A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057984



Internal ID18800515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10443029..10558343hg38UCSC Ensembl
Innerchr21:10954114..11069428hg19UCSC Ensembl
Innerchr21:9975985..10091299hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38115315
hg19115315
hg18115315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4363n100
Supporting Variantsnssv3732543, nssv3732542
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)nsv1057984
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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