A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036368



Internal ID19125587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93121559..93140356hg38UCSC Ensembl
Innerchr15:93664788..93683585hg19UCSC Ensembl
Innerchr15:91465792..91484589hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3818798
hg1918798
hg1818798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555235
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)nsv1036368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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