A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547726



Internal ID18846007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32329014hg38UCSC Ensembl
Innerchr15:32458661..32621215hg19UCSC Ensembl
Innerchr15:30245953..30408507hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38162555
hg19162555
hg18162555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035202
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547726
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