A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11145n54



Internal ID22779040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2628411..2659000hg38UCSC Ensembl
chr7:2668045..2698634hg19UCSC Ensembl
chr7:2634571..2665160hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3830590
hg1930590
hg1830590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605868, nsv605866
Samples
Known GenesTTYH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11145n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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