A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11620n54



Internal ID20145044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137198178..137250712hg38UCSC Ensembl
chr7:136882925..136935459hg19UCSC Ensembl
chr7:136533465..136585999hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3852535
hg1952535
hg1852535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608464, nsv608465
Samples
Known GenesPTN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11620n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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