A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552214



Internal ID15992937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119100409..119209705hg38UCSC Ensembl
Innerchr10:120859921..120969217hg19UCSC Ensembl
Innerchr10:120849911..120959207hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38109297
hg19109297
hg18109297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv758794
Samples
Known GenesFAM45A, FAM45B, GRK5, PRDX3, SFXN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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