A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525041



Internal ID15452334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54776011..54844557hg38UCSC Ensembl
Innerchr15:55068209..55136755hg19UCSC Ensembl
Innerchr15:52855501..52924047hg18UCSC Ensembl
Innerchr15:52855501..52924047hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3868547
hg1968547
hg1868547
hg1768547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701085
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525041
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer