A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550160



Internal ID16337569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20542667..20565668hg38UCSC Ensembl
Innerchr10:20831596..20854597hg19UCSC Ensembl
Innerchr10:20871602..20894603hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3823002
hg1923002
hg1823002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv992n54
Supporting Variantsnssv1174153, nssv744345
Samples1780854455_A
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550160
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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