A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719897



Internal ID15667167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103611144..103682046hg38UCSC Ensembl
Innerchr1:104153766..104224668hg19UCSC Ensembl
Innerchr1:103955289..104026191hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3870903
hg1970903
hg1870903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547043
Supporting Variants
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)nssv719897
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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