A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551179



Internal ID16338588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62202267..62248549hg38UCSC Ensembl
Innerchr10:63962026..64008308hg19UCSC Ensembl
Innerchr10:63632032..63678314hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3846283
hg1946283
hg1846283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748924
Samples
Known GenesRTKN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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