A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710534



Internal ID15657804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15683836..15684641hg38UCSC Ensembl
Innerchr1:16010331..16011136hg19UCSC Ensembl
Innerchr1:15882918..15883723hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545611
Supporting Variants
Samples
Known GenesPLEKHM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710534
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