A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044844



Internal ID18787375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33773323..34004628hg38UCSC Ensembl
Innerchr15:34065524..34296829hg19UCSC Ensembl
Innerchr15:31852816..32084121hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38231306
hg19231306
hg18231306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3547872
Samples
Known GenesAVEN, CHRM5, RYR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044844
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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