A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065989



Internal ID19155208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20299192..20838659hg38UCSC Ensembl
Innerchr21:21671504..22210977hg19UCSC Ensembl
Innerchr21:20593375..21132848hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38539468
hg19539474
hg18539474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4398n100
Supporting Variantsnssv3599832
Samples
Known GenesLINC00320
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065989
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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