A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038603



Internal ID19127822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85919621..85950208hg38UCSC Ensembl
Innerchr15:86462852..86493439hg19UCSC Ensembl
Innerchr15:84263856..84294443hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3830588
hg1930588
hg1830588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555094
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)nsv1038603
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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