A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039818



Internal ID18782349
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 StatusM
Merged Variantsdgv2583n100
Supporting Variantsnssv3552281
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)nsv1039818
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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