A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055386



Internal ID19144605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:22048601..22185744hg38UCSC Ensembl
Innerchr21:23420920..23558063hg19UCSC Ensembl
Innerchr21:22342791..22479934hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38137144
hg19137144
hg18137144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599886
Samples
Known GenesLINC00308
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055386
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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