A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547121



Internal ID15987844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103623702..103756622hg38UCSC Ensembl
Innerchr1:104166324..104299244hg19UCSC Ensembl
Innerchr1:103967847..104100767hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38132921
hg19132921
hg18132921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv401n54
Supporting Variantsnssv720086, nssv720085, nssv720084
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)nsv547121
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer