A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036168



Internal ID19125387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60172801..60238144hg38UCSC Ensembl
Innerchr15:60465000..60530343hg19UCSC Ensembl
Innerchr15:58252292..58317635hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3865344
hg1965344
hg1865344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2610n100
Supporting Variantsnssv3553617
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)nsv1036168
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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