A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056588



Internal ID19145807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14210910..14243199hg38UCSC Ensembl
Innerchr21:15583231..15615520hg19UCSC Ensembl
Innerchr21:14505102..14537391hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3832290
hg1932290
hg1832290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586455
Samples
Known GenesRBM11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056588
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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