A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038989



Internal ID19128208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23802041..23814160hg38UCSC Ensembl
Innerchr15:24047188..24059307hg19UCSC Ensembl
Innerchr15:21598281..21610400hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3812120
hg1912120
hg1812120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3538887
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)nsv1038989
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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