A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550729



Internal ID16338138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47620818..47720438hg38UCSC Ensembl
Innerchr10:47310831..47410458hg19UCSC Ensembl
Innerchr10:46730837..46830464hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3899621
hg1999628
hg1899628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747372
Samples
Known GenesFAM35DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550729
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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