A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844425



Internal ID16138381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183826..71184937hg38UCSC Ensembl
Innerchr15:71476165..71477276hg19UCSC Ensembl
Innerchr15:69263219..69264330hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381112
hg191112
hg181112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569830
Supporting Variants
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844425
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