A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548058



Internal ID15988781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:160955665..161019824hg38UCSC Ensembl
Innerchr1:160925455..160989614hg19UCSC Ensembl
Innerchr1:159192079..159256238hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3864160
hg1964160
hg1864160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727676
Samples
Known GenesF11R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548058
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