A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551801



Internal ID16339210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942524..86942906hg38UCSC Ensembl
Innerchr10:88702281..88702663hg19UCSC Ensembl
Innerchr10:88692261..88692643hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38383
hg19383
hg18383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1324n54
Supporting Variantsnssv752244
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551801
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