A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575569



Internal ID16362978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53238476..53299659hg38UCSC Ensembl
Innerchr17:51315837..51377020hg19UCSC Ensembl
Innerchr17:48670836..48732019hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3861184
hg1961184
hg1861184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149772
SamplesNINDS_94
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575569
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