A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11244n54



Internal ID20144668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27095695..27157700hg38UCSC Ensembl
chr7:27135314..27197319hg19UCSC Ensembl
chr7:27101839..27163844hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3862006
hg1962006
hg1862006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606466, nsv606463, nsv606467
Samples
Known GenesHOTAIRM1, HOXA1, HOXA2, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA-AS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11244n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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