A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869529



Internal ID15816799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31313044..31322205hg38UCSC Ensembl
Innerchr17:29640062..29649223hg19UCSC Ensembl
Innerchr17:26664188..26673349hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389162
hg199162
hg189162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574674
Supporting Variants
Samples
Known GenesEVI2A, EVI2B, NF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869529
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