A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060055



Internal ID19149274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21049623..21111546hg38UCSC Ensembl
Innerchr22:21403912..21465835hg19UCSC Ensembl
Innerchr22:19733912..19795835hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3861924
hg1961924
hg1861924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3587390
Samples
Known GenesBCRP2, LOC400891
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060055
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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