A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555287



Internal ID18853568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97321333..97391630hg38UCSC Ensembl
Innerchr15:97864563..97934860hg19UCSC Ensembl
Innerchr15:95665567..95735864hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3870298
hg1970298
hg1870298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048405
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555287
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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