A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547062



Internal ID15987785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103611243..103727325hg38UCSC Ensembl
Innerchr1:104153865..104269947hg19UCSC Ensembl
Innerchr1:103955388..104071470hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38116083
hg19116083
hg18116083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv420n54
Supporting Variantsnssv719990
Samples
Known GenesAMY1A, AMY1B, AMY1C, AMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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