A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547957



Internal ID16335366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:154502054..154502561hg38UCSC Ensembl
Innerchr1:154474530..154475037hg19UCSC Ensembl
Innerchr1:152741154..152741661hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38508
hg19508
hg18508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv724904
Samples
Known GenesTDRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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