A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11605n54



Internal ID22779500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123320321..123391378hg38UCSC Ensembl
chr7:122960375..123031432hg19UCSC Ensembl
chr7:122747611..122818668hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3871058
hg1971058
hg1871058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608337, nsv608336
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11605n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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