A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10758n54



Internal ID20144182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69948540..70030414hg38UCSC Ensembl
chr6:70658432..70740306hg19UCSC Ensembl
chr6:70715153..70797027hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3881875
hg1981875
hg1881875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603638, nsv603637
Samples
Known GenesCOL19A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10758n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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