A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545693



Internal ID18497288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30440064hg38UCSC Ensembl
Innerchr15:30386399..30732267hg19UCSC Ensembl
Innerchr15:28173691..28519559hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38345869
hg19345869
hg18345869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050209
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545693
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