A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573962



Internal ID16361371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:310060..356254hg38UCSC Ensembl
Innerchr17:159851..206045hg19UCSC Ensembl
Innerchr17:159851..206045hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3846195
hg1946195
hg1846195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv864420
Samples
Known GenesLOC100506388, RPH3AL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573962
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