A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549906



Internal ID16337315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5878873..5896581hg38UCSC Ensembl
Innerchr10:5920836..5938544hg19UCSC Ensembl
Innerchr10:5960842..5978550hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3817709
hg1917709
hg1817709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743524
Samples
Known GenesANKRD16, FBXO18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549906
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