A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876240



Internal ID16170196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77270619..77275705hg38UCSC Ensembl
Innerchr17:75266701..75271787hg19UCSC Ensembl
Innerchr17:72778296..72783382hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg385087
hg195087
hg185087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576083
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876240
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