A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039758



Internal ID19128977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36075308..36101269hg38UCSC Ensembl
Innerchr15:36367509..36393470hg19UCSC Ensembl
Innerchr15:34154801..34180762hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3825962
hg1925962
hg1825962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552231
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)nsv1039758
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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