A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11742n54



Internal ID22779637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154880936..154909643hg38UCSC Ensembl
chr7:154672646..154701353hg19UCSC Ensembl
chr7:154303579..154332286hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3828708
hg1928708
hg1828708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609113, nsv609115, nsv609114
SamplesHGDP01163, NINDS_66
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11742n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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