A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552233



Internal ID18850514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36213837..36252547hg38UCSC Ensembl
Innerchr15:36506038..36544748hg19UCSC Ensembl
Innerchr15:34293330..34332040hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3838711
hg1938711
hg1838711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044541
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)nssv3552233
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