A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055991



Internal ID19145210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20299192..20844801hg38UCSC Ensembl
Innerchr21:21671504..22217119hg19UCSC Ensembl
Innerchr21:20593375..21138990hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38545610
hg19545616
hg18545616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4398n100
Supporting Variantsnssv3732675
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)nsv1055991
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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