A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551052



Internal ID16338461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55649935..55777402hg38UCSC Ensembl
Innerchr10:57409695..57537162hg19UCSC Ensembl
Innerchr10:57079701..57207168hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38127468
hg19127468
hg18127468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748552
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551052
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