A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050740



Internal ID18793271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89006295..89155865hg38UCSC Ensembl
Innerchr15:89549526..89699096hg19UCSC Ensembl
Innerchr15:87350530..87500100hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38149571
hg19149571
hg18149571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718186
Samples
Known GenesABHD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050740
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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