A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601482



Internal ID16388891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30879053..30886313hg38UCSC Ensembl
Innerchr6:30846830..30854090hg19UCSC Ensembl
Innerchr6:30954809..30962069hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg387261
hg197261
hg187261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1052262
Samples
Known GenesDDR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601482
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