A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604329



Internal ID16391738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102604238..102688773hg38UCSC Ensembl
Innerchr6:103052113..103136648hg19UCSC Ensembl
Innerchr6:103158806..103243341hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3884536
hg1984536
hg1884536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155091
Samples1780854495_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604329
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