A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042097



Internal ID19131316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85796276..85806808hg38UCSC Ensembl
Innerchr15:86339507..86350039hg19UCSC Ensembl
Innerchr15:84140511..84151043hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3810533
hg1910533
hg1810533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2652n100
Supporting Variantsnssv3555088
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)nsv1042097
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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