A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057883



Internal ID19147102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10511867..10775598hg38UCSC Ensembl
Innerchr21:10736859..11000590hg19UCSC Ensembl
Innerchr21:9758730..10022461hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38263732
hg19263732
hg18263732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4353n100
Supporting Variantsnssv3583664
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057883
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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