A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551538



Internal ID15992261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76492431..76500629hg38UCSC Ensembl
Innerchr10:78252189..78260387hg19UCSC Ensembl
Innerchr10:77922195..77930393hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg388199
hg198199
hg188199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750296, nssv750297, nssv750298
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551538
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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