A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550726



Internal ID15991449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46396625..46489856hg38UCSC Ensembl
Innerchr10:47041592..47153137hg19UCSC Ensembl
Innerchr10:46461598..46573143hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3893232
hg19111546
hg18111546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747369
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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