A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552215



Internal ID15992938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119531059..119587817hg38UCSC Ensembl
Innerchr10:121290571..121347329hg19UCSC Ensembl
Innerchr10:121280561..121337319hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3856759
hg1956759
hg1856759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv758795
Samples
Known GenesRGS10, TIAL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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