A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066853



Internal ID19156072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47525232..47544679hg38UCSC Ensembl
Innerchr22:47920981..47940428hg19UCSC Ensembl
Innerchr22:46299645..46319092hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3819448
hg1919448
hg1819448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592272
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066853
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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