A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604444



Internal ID16391853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107114286..107115146hg38UCSC Ensembl
Innerchr6:107435490..107436350hg19UCSC Ensembl
Innerchr6:107542183..107543043hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38861
hg19861
hg18861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10897n54
Supporting Variantsnssv1071894
Samples
Known GenesBEND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604444
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer