A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601245



Internal ID16388654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29905273hg38UCSC Ensembl
Innerchr6:29851443..29873050hg19UCSC Ensembl
Innerchr6:29959422..29981029hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3821608
hg1921608
hg1821608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10345n54
Supporting Variantsnssv1051737
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601245
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