A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602092



Internal ID16389501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32020762..32028820hg38UCSC Ensembl
Innerchr6:31988539..31996597hg19UCSC Ensembl
Innerchr6:32096517..32104592hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388059
hg198059
hg188076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10484n54
Supporting Variantsnssv1053884, nssv1053889, nssv1053887, nssv1053888, nssv1053881, nssv1053890, nssv1053882, nssv1053886, nssv1053885, nssv1053891, nssv1053883
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602092
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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