A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547126



Internal ID15987849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103624903..103654458hg38UCSC Ensembl
Innerchr1:104167525..104197080hg19UCSC Ensembl
Innerchr1:103969048..103998603hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3829556
hg1929556
hg1829556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv432n54
Supporting Variantsnssv720091
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547126
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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