A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604407



Internal ID16045130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104813034..104814306hg38UCSC Ensembl
Innerchr6:105260909..105262181hg19UCSC Ensembl
Innerchr6:105367602..105368874hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381273
hg191273
hg181273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10891n54
Supporting Variantsnssv1071691, nssv1071692
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604407
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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