A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552281



Internal ID18503876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43553212..43696343hg38UCSC Ensembl
Innerchr15:43845410..43988541hg19UCSC Ensembl
Innerchr15:41632702..41775833hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38143132
hg19143132
hg18143132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039818
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1A, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552281
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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