A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3553662



Internal ID18505257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69204723..69258106hg38UCSC Ensembl
Innerchr15:69497062..69550445hg19UCSC Ensembl
Innerchr15:67284116..67337499hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853384
hg1953384
hg1853384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039652
Supporting Variants
Samples
Known GenesGLCE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3553662
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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