A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050892



Internal ID18793423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41836657..41894284hg38UCSC Ensembl
Innerchr15:42128855..42186482hg19UCSC Ensembl
Innerchr15:39916147..39973774hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3857628
hg1957628
hg1857628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552275
Samples
Known GenesJMJD7, JMJD7-PLA2G4B, MIR4310, PLA2G4B, SPTBN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050892
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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