A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546441



Internal ID16333850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66490195..66503401hg38UCSC Ensembl
Innerchr1:66955878..66969084hg19UCSC Ensembl
Innerchr1:66728466..66741672hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3813207
hg1913207
hg1813207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173007
Samples1798860592_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546441
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