A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581756



Internal ID16369165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:47325567..47363791hg38UCSC Ensembl
Innerchr2:47552706..47590930hg19UCSC Ensembl
Innerchr2:47406210..47444434hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3838225
hg1938225
hg1838225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908107
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581756
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