A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875908



Internal ID16169864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68112848..68187221hg38UCSC Ensembl
Innerchr17:66108989..66183362hg19UCSC Ensembl
Innerchr17:63620627..63694957hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3874374
hg1974374
hg1874331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575926
Supporting Variants
Samples
Known GenesLINC00674
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875908
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