A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601505



Internal ID16388914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269628..31270746hg38UCSC Ensembl
Innerchr6:31237405..31238523hg19UCSC Ensembl
Innerchr6:31345384..31346502hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10371n54
Supporting Variantsnssv1052336, nssv1052344, nssv1052334, nssv1052329, nssv1052335, nssv1052348, nssv1052331, nssv1052347, nssv1052340, nssv1052342, nssv1052328, nssv1052332, nssv1052339, nssv1052345, nssv1052327, nssv1052337, nssv1052338, nssv1052343, nssv1052341, nssv1052330, nssv1052333, nssv1052349, nssv1052346
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601505
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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