A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv865848



Internal ID16159804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:947302..949579hg38UCSC Ensembl
Innerchr17:850542..852819hg19UCSC Ensembl
Innerchr17:797292..799569hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382278
hg192278
hg182278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574102
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv865848
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