A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602414



Internal ID16389823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32521954..32538126hg38UCSC Ensembl
Innerchr6:32489731..32505903hg19UCSC Ensembl
Innerchr6:32597709..32613881hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3816173
hg1916173
hg1816173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055516
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602414
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