A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058946



Internal ID19148165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35501977..35530772hg38UCSC Ensembl
Innerchr22:35898024..35926819hg19UCSC Ensembl
Innerchr22:34227970..34256765hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3828796
hg1928796
hg1828796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734208
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)nsv1058946
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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