A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844332



Internal ID15791602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67576449..67576686hg38UCSC Ensembl
Innerchr15:67868787..67869024hg19UCSC Ensembl
Innerchr15:65655841..65656078hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38238
hg19238
hg18238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569801
Supporting Variants
Samples
Known GenesMAP2K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844332
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