A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549751



Internal ID16337160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:267364..688289hg38UCSC Ensembl
Innerchr10:313304..734229hg19UCSC Ensembl
Innerchr10:303304..724229hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38420926
hg19420926
hg18420926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174093
SamplesHGDP00728
Known GenesDIP2C, MIR5699, PRR26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549751
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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