A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550198



Internal ID16337607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20573498..20639436hg38UCSC Ensembl
Innerchr10:20862427..20928365hg19UCSC Ensembl
Innerchr10:20902433..20968371hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3865939
hg1965939
hg1865939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1001n54
Supporting Variantsnssv744699
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer