A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560638



Internal ID16348047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128177571..128203476hg38UCSC Ensembl
Innerchr12:128662116..128688021hg19UCSC Ensembl
Innerchr12:127228069..127253974hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3825906
hg1925906
hg1825906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv804215
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560638
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