A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545777



Internal ID15986500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23874116..23874672hg38UCSC Ensembl
Innerchr1:24200606..24201162hg19UCSC Ensembl
Innerchr1:24073193..24073749hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38557
hg19557
hg18557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv190n54
Supporting Variantsnssv711331
Samples
Known GenesCNR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545777
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