A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552289



Internal ID15993012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124875780..124998761hg38UCSC Ensembl
Innerchr10:126564349..126687330hg19UCSC Ensembl
Innerchr10:126554339..126677320hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38122982
hg19122982
hg18122982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760492
Samples
Known GenesCTBP2, ZRANB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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