A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11759n54



Internal ID22779654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156594543..156611368hg38UCSC Ensembl
chr7:156387237..156404062hg19UCSC Ensembl
chr7:156079998..156096823hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3816826
hg1916826
hg1816826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609208, nsv609186
Samples
Known GenesLINC01006
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11759n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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