A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044299



Internal ID19133518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46797455..46827738hg38UCSC Ensembl
Innerchr15:47089653..47119936hg19UCSC Ensembl
Innerchr15:44876945..44907228hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3830284
hg1930284
hg1830284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716723, nssv3552371
Samples
Known GenesMIR548A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044299
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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