A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602954



Internal ID16390363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37534809..37549709hg38UCSC Ensembl
Innerchr6:37502585..37517485hg19UCSC Ensembl
Innerchr6:37610563..37625463hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3814901
hg1914901
hg1814901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154304
Samples1780862306_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602954
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