A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551922



Internal ID16339331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91908383..91908906hg38UCSC Ensembl
Innerchr10:93668140..93668663hg19UCSC Ensembl
Innerchr10:93658120..93658643hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38524
hg19524
hg18524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753955
Samples
Known GenesFGFBP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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