A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059410



Internal ID19148629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25268006..25531841hg38UCSC Ensembl
Innerchr22:25663973..25927808hg19UCSC Ensembl
Innerchr22:23993973..24257808hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38263836
hg19263836
hg18263836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4547n100
Supporting Variantsnssv3600476, nssv3600473, nssv3600474, nssv3600472, nssv3600475
Samples
Known GenesCRYBB2P1, IGLL3P, 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)nsv1059410
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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