A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11158n54



Internal ID19003334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3752406..3812629hg38UCSC Ensembl
chr7:3792038..3852261hg19UCSC Ensembl
chr7:3758564..3818787hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3860224
hg1960224
hg1860224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605938, nsv605937
Samples
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11158n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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