A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058986



Internal ID19148205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10548957..10775598hg38UCSC Ensembl
Innerchr21:10736859..10963500hg19UCSC Ensembl
Innerchr21:9758730..9985371hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38226642
hg19226642
hg18226642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4350n100
Supporting Variantsnssv3583621, nssv3732468
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)nsv1058986
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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