A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5438n54



Internal ID22773333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6189226..6232520hg38UCSC Ensembl
chr17:6092546..6135840hg19UCSC Ensembl
chr17:6033270..6076564hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3843295
hg1943295
hg1843295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574313, nsv574314
SamplesHGDP01264
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5438n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer