A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546694



Internal ID18498289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30281095..30487376hg38UCSC Ensembl
Innerchr15:30573298..30779579hg19UCSC Ensembl
Innerchr15:28360590..28566871hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38206282
hg19206282
hg18206282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052716
Supporting Variants
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3546694
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