A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552442



Internal ID15993165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131112791..131114251hg38UCSC Ensembl
Innerchr10:132911054..132912514hg19UCSC Ensembl
Innerchr10:132801044..132802504hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381461
hg191461
hg181461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv761621, nssv761622
Samples
Known GenesTCERG1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552442
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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