A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546981



Internal ID15987704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103579934..103630590hg38UCSC Ensembl
Innerchr1:104122556..104173212hg19UCSC Ensembl
Innerchr1:103924079..103974735hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3850657
hg1950657
hg1850657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv400n54
Supporting Variantsnssv719765
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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