A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065662



Internal ID19154881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25326305..25521763hg38UCSC Ensembl
Innerchr22:25722272..25917730hg19UCSC Ensembl
Innerchr22:24052272..24247730hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38195459
hg19195459
hg18195459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4552n100
Supporting Variantsnssv3600683
Samples
Known GenesCRYBB2P1, LRP5L, MIR6817
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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