A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058925



Internal ID19148144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48361764..48449692hg38UCSC Ensembl
Innerchr22:48757576..48845504hg19UCSC Ensembl
Innerchr22:47136240..47224168hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3887929
hg1987929
hg1887929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592280
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)nsv1058925
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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