A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551635



Internal ID15992358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79925268..80212630hg38UCSC Ensembl
Innerchr10:81685024..81972386hg19UCSC Ensembl
Innerchr10:81675004..81962366hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38287363
hg19287363
hg18287363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751848
Samples
Known GenesANXA11, LINC00857, LOC100288974, PLAC9, SFTPD, TMEM254, TMEM254-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551635
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