A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978169



Internal ID12634846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25254681..25519883hg38UCSC Ensembl
Innerchr22:25650648..25915850hg19UCSC Ensembl
Innerchr22:23980648..24245850hg18UCSC Ensembl
Innerchr22:23975202..24240404hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38265203
hg19265203
hg18265203
hg17265203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35154
Supporting Variants
SamplesNA18973
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978169
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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