A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875720



Internal ID15822990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61042000..61049006hg38UCSC Ensembl
Innerchr17:59119361..59126367hg19UCSC Ensembl
Innerchr17:56474143..56481149hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg387007
hg197007
hg187007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575832
Supporting Variants
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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