A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604330



Internal ID16391739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102698199..102795157hg38UCSC Ensembl
Innerchr6:103146074..103243032hg19UCSC Ensembl
Innerchr6:103252767..103349725hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3896959
hg1996959
hg1896959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070913
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604330
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