A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049319



Internal ID19138538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53379748..53493070hg38UCSC Ensembl
Innerchr15:53671945..53785267hg19UCSC Ensembl
Innerchr15:51459237..51572559hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38113323
hg19113323
hg18113323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2600n100
Supporting Variantsnssv3552420
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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