A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5739n54



Internal ID20139163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61044669..61051300hg38UCSC Ensembl
chr17:59122030..59128661hg19UCSC Ensembl
chr17:56476812..56483443hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg386632
hg196632
hg186632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575837, nsv575836
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5739n54
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