A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751964



Internal ID12638830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36137737..36183513hg38UCSC Ensembl
Innerchr22:36533785..36579561hg19UCSC Ensembl
Innerchr22:34863731..34909507hg18UCSC Ensembl
Innerchr22:34858285..34904061hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3845777
hg1945777
hg1845777
hg1745777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6985383, essv6985381, essv6990125, essv6985382
SamplesSPC_157
Known GenesAPOL3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751964
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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