A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551241



Internal ID16338650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65141812..65251930hg38UCSC Ensembl
Innerchr10:66901570..67011688hg19UCSC Ensembl
Innerchr10:66571576..66681694hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38110119
hg19110119
hg18110119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv749369
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551241
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